90 FR 54 pgs. 13371-13375 - Over-the-Counter Monograph Drug User Fee Program—Facility Fee Rates for Fiscal Year 2025
Type: NOTICEVolume: 90Number: 54Pages: 13371 - 13375
Pages: 13371, 13372, 13373, 13374, 13375Docket number: [Docket No. FDA-2025-N-0648]
FR document: [FR Doc. 2025-04860 Filed 3-20-25; 8:45 am]
Agency: Health and Human Services Department
Sub Agency: Food and Drug Administration
Official PDF Version: PDF Version
[top]
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2025-N-0648]
Over-the-Counter Monograph Drug User Fee Program-Facility Fee Rates for Fiscal Year 2025
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice.
SUMMARY:
The Food and Drug Administration (FDA, the Agency, or we) is announcing the over-the-counter (OTC) monograph drug facility (MDF) fee rates under the OTC monograph drug user fee program (OMUFA) for fiscal year (FY) 2025. The Federal Food, Drug, and Cosmetic Act (FD&C Act) authorizes FDA to assess and collect user fees from qualifying manufacturers of OTC monograph drugs and submitters of OTC monograph order requests (OMORs). This notice publishes the OMUFA facility fee rates for FY 2025.
DATES:
These facility fees are effective on October 1, 2024, and will remain in effect through September 30, 2025.
FOR FURTHER INFORMATION CONTACT:
Olufunmilayo Ariyo, Office of Financial Management, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20993, 240-402-4989; or the User Fees Support Staff at OO-OFBA-OFM-UFSS-Government@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Section 744M of the FD&C Act (21 U.S.C. 379j-72), authorizes FDA to assess and collect: (1) facility fees from qualifying owners of OTC monograph drug facilities and (2) fees from submitters of qualifying OTC OMORs. The OTC OMOR fee rates for FY 2025 were published on July 31, 2024. 1 OMUFA fees are to support FDA's OTC monograph drug activities, which are detailed in section 744L(6) of the FD&C Act (21 U.S.C. 379j-71(6)) and include various FDA activities associated with OTC monograph drugs. For OMUFA purposes:
Footnotes:
1 ? https://www.federalregister.gov/documents/2024/07/31/2024-16878/over-the-counter-monograph-drug-user-fee-program-otc-monograph-order-request-fee-rates-for-fiscal.
• An OTC monograph drug is a nonprescription drug without an approved new drug application that is governed by the provisions of section 505G of the FD&C Act (21 U.S.C. 355h) (see section 744L(5) of the FD&C Act);
• An OTC MDF is a foreign or domestic business or other entity that, in addition to meeting other criteria, is engaged in manufacturing or processing the finished dosage form of an OTC monograph drug (see section 744L(10) of the FD&C Act); and
• A contract manufacturing organization (CMO) facility is an OTC monograph drug facility where neither the owner nor any affiliate of the owner or facility sells the OTC monograph drug produced at such facility directly to wholesalers, retailers, or consumers in the United States (see section 744L(2) of the FD&C Act).
Under section 744M(a)(1)(A) of the FD&C Act, a facility fee for FY 2025 shall be assessed with respect to each facility that is identified as an OTC monograph drug facility during the fee-liable period from January 1, 2024, through December 31, 2024. 2 Consistent with the statute, FDA will assess and collect facility fees with respect to the two types of OTC monograph drug facilities-MDF and CMO facilities. A full facility fee will be assessed to each qualifying person that owns a facility identified as an MDF (see section 744M(a)(1)(A) of the FD&C Act), and a reduced facility fee of two-thirds will be assessed to each qualifying person that owns a facility identified as a CMO facility (see section 744M(a)(1)(B)(ii) of the FD&C Act). The facility fees for FY 2025 are due on June 2, 2025 (see section 744M(a)(1)(D)(ii) of the FD&C Act). 3
Footnotes:
2 ?Under section 744M(a)(1) of the FD&C Act, "Each person that owns a facility identified as an OTC monograph drug facility on December 31 of the fiscal year or at any time during the preceding 12-month period shall be assessed an annual fee for each such facility." For purposes of FY 2025 facility fees, that time period is January 1, 2024, through December 31, 2024.
3 ?Assuming that, as we anticipate, the FY 2025 fee appropriation will occur prior to June 3, 2025. Under section 744M(a)(1)(D)(ii), the FY 2025 facility fees are due on the later of: (1) the first business day of June 2025 ( i.e., June 3, 2025) or (2) the first business day after the enactment of an appropriations Act providing for the collection and obligation of FY 2025 OMUFA fees.
As discussed in greater detail below:
• OTC monograph drug facilities are exempt from FY 2025 facility fees if they had ceased OTC monograph drug activities, and updated their registration with FDA to that effect, prior to December 31, 2023 (see section 744M(a)(1)(B)(i) of the FD&C Act).
[top] • Entities that registered with FDA during the Coronavirus Disease 2019 (COVID-19) pandemic whose sole activity with respect to OTC monograph drugs during the pandemic consisted of manufacturing OTC hand sanitizer
Footnotes:
4 ?The term "hand sanitizer" commonly refers to consumer antiseptic rubs. However, because the Department of Health and Human Services (HHS) notice published January 12, 2021, referred to "persons that entered the over-the-counter drug market to supply hand sanitizer products in response to the COVID-19 Public Health Emergency" (86 FR 2420, https://www.federalregister.gov/documents/2021/01/12/2021-00237/notice-that-persons-that-entered-the-over-the-counter-drug-market-to-supply-hand-sanitizer-during ), we are using the same terminology-"hand sanitizer products"-to refer to OTC monograph drug products intended for use (without water) as antiseptic hand rubs or antiseptic hand wipes by consumers or healthcare personnel.
5 ?See HHS Federal Register notice of January 12, 2021, 86 FR 2420, https://www.federalregister.gov/documents/2021/01/12/2021-00237/notice-that-persons-that-entered-the-over-the-counter-drug-market-to-supply-hand-sanitizer-during.
For FY 2025, the OMUFA facility fee rates are: MDF facility fees ($37,556) and CMO facility fees ($25,037). These fees are effective for the period from October 1, 2024, through September 30, 2025. 6 This document is issued pursuant to section 744M(a)(4) and 744M(c)(4)(B) of the FD&C Act and describes the calculations used to set the OMUFA facility fees for FY 2025 in accordance with the directives in the statute.
Footnotes:
6 ?These OMUFA facility fees are for FY 2025, per section 744M(a) of the FD&C Act.
II. Facility Fee Revenue Amount for FY 2025
A. Base Fee Revenue Amount
Under OMUFA, FDA sets annual facility fees to generate the total facility fee revenues for each fiscal year established by section 744M(b) of the FD&C Act. The yearly base revenue amount is the starting point for setting annual facility fee rates. The base revenue for FY 2025 is the dollar amount of the total revenue amount for the previous fiscal year, without certain adjustments made for that previous year, and is $29,253,365 (see section 744M(b)(3)(B) of the FD&C Act).
B. Fee Revenue Adjustment for Inflation
Under OMUFA, the annual base revenue amount for facility fees is adjusted for inflation for FY 2025, per section 744M(c)(1) of the FD&C Act. That provision states that the dollar amount of the inflation adjustment is equal to the product of the annual base revenue for the fiscal year and the inflation adjustment percentage. For FY 2025 the inflation adjustment percentage is the sum of:
• (I) the average annual percent change in cost, per full-time equivalent (FTE) position of FDA, of all personnel compensation and benefits paid with respect to such positions for the first 3 years of the preceding 4 fiscal years, multiplied by the proportion of personnel compensation and benefits (PC&B) costs to total costs of the OTC monograph drug activities for the first 3 years of the preceding 4 fiscal years (see section 744M(c)(1)(C)(ii)(I) of the FD&C Act); and
• (II) the average annual percent change that occurred in the Consumer Price Index (CPI) for urban consumers (Washington-Baltimore, DC-MD-VA-WV; Not Seasonally Adjusted; All items; Annual Index) for the first 3 years of the preceding 4 years of available data multiplied by the proportion of all costs other than personnel compensation and benefits costs to total costs of OTC monograph drug activities for the first 3 years of the preceding 4 fiscal years (see section 744M(c)(1)(C)(ii)(II) of the FD&C Act).
As a result of a geographical revision made by the Bureau of Labor and Statistics in January 2018, the "Washington, DC-Baltimore" index was discontinued and replaced with two separate indices ( i.e., the "Washington-Arlington-Alexandria" and "Baltimore-Columbia-Towson" indices). To continue applying a CPI that best reflects the geographic region in which FDA is located and that provides the most current data available, the "Washington-Arlington-Alexandria" index is used in calculating the inflation adjustment percentage.
Table 1 summarizes the actual cost and FTE data for the specified fiscal years, provides the percent changes from the previous fiscal years, and provides the average percent changes over the first 3 of the 4 fiscal years preceding FY 2025. The 3-year average is 3.8539 percent.
| Fiscal year | 2021 | 2022 | 2023 | 3-Year average |
|---|---|---|---|---|
| Total PC&B | 3,039,513,000 | 3,165,477,000 | 3,436,513,000 | 3.8539% |
| Total FTE | 18,501 | 18,474 | 18,729 | |
| PC&B per FTE | 164,289 | 171,348 | 183,486 | |
| Percent Change From Previous Year | 0.1811% | 4.2967% | 7.0838% |
Under the statute, this 3.8539 percent is multiplied by the proportion of PC&B costs to the total FDA costs of OTC Monograph drug activities for the first 3 years of the preceding 4 fiscal years (see section 744M(c)(1)(C)(ii) of the FD&C Act).
Table 2 shows the PC&B and the total obligations for OTC monograph drug activities for the first 3 of the preceding 4 fiscal years.
| Fiscal year | 2021 | 2022 | 2023 | 3-Year average |
|---|---|---|---|---|
| Total PC&B | 23,133,775 | 25,415,237 | 39,133,075 | 58.1262% |
| Total Costs | 35,030,659 | 49,644,273 | 68,480,052 | |
| PC&B Percent | 66.0378% | 51.1947% | 57.1452% |
The payroll adjustment is 3.8539 percent from table 1 multiplied by 58.1262 percent from table 2 resulting in 2.2401 percent.
[top] Table 3 provides the summary data for the percent changes in the specified
| Year | 2021 | 2022 | 2023 | 3-Year average |
|---|---|---|---|---|
| Annual CPI | 277.73 | 296.12 | 305.32 | 4.5616% |
| Annual Percent Change | 3.9568% | 6.6212% | 3.1069% |
The statute specifies that this 4.5616 percent be multiplied by the proportion of all costs other than PC&B to total costs of OTC monograph drug activities for the first 3 years of the preceding 4 fiscal years. Because 58.1262 percent was obligated for PC&B (as shown in table 2), 41.8738 percent is the portion of costs other than PC&B (100 percent minus 58.1262 percent equals 41.8738 percent). The nonpayroll adjustment is 4.5616 percent times 41.8738 percent, or 1.9101 percent.
Next, we add the payroll adjustment (2.2401 percent) to the nonpayroll adjustment (1.9101 percent), for a total inflation adjustment of 4.1502 percent (rounded) for FY 2025.
Pursuant to the statute, the FY 2025 base revenue of $29,253,365 is increased by the total inflation adjustment of 4.1502 percent, yielding an inflation adjusted base revenue amount of $30,467,438 for FY 2025 (see section 744M(c)(1)(A)).
C. Additional Dollar Amounts
For FY 2025, the inflation adjusted revenue amount of $30,467,438 is increased by an additional dollar amount of $3 million as specified in the statute (see section 744M(b)(2)(E) of the FD&C Act). This yields an adjusted fee revenue subtotal of $33,467,438.
D. Fee Revenue Adjustment for Additional Direct Cost
Fee revenue is further adjusted for additional direct costs as specified in the statute. In FY 2025, $3 million is added to the facility fee revenues to account for additional direct costs (see section 744M(c)(3)(E) of the FD&C Act). Adding the additional direct costs amount of $3 million to $33,467,438 yields an additional direct cost adjusted fee revenue of $36,467,438.
E. Fee Revenue Adjustment for Operating Reserve
Under OMUFA, FDA may further increase the FY 2025 facility fee revenue and fees if such an adjustment is necessary to provide up to 10 weeks of operating reserves of carryover user fees for OTC monograph drug activities (see section 744M(c)(2)(B) of the FD&C Act). Accordingly, in setting fees for FY 2025, the Agency must estimate its carryover for FY 2025 to ensure the Agency has sufficient carryover to continue its OTC monograph drug activities, as required under the statute, including an operating reserve to mitigate certain financial risks, such as under collections, unanticipated surges in program costs, or a lapse in appropriations. Under the statute, if FDA has carryover for OTC monograph drug activities that would exceed 10 weeks of such operating reserves, FDA is required to decrease FY 2025 fee revenues and fees to provide for not more than 10 weeks of operating reserves of carryover user fees (see section 744M(c)(2)(C) of the FD&C Act).
Per the statute, OMUFA facility fees are not due until the third quarter of each fiscal year ( i.e., the first business day in June). To address this timing of facility fee collections for late in the fiscal year, the Agency must set aside additional carryover, beyond that for an operating reserve, to sustain the Agency's OTC monograph drug activities until the facility fees for the subsequent fiscal year are due and payable on the first business day in June ( i.e., June 1, 2026). Thus, the Agency will require FY 2025 carryover sufficient to cover payroll and operating expenses for the first 8 months ( i.e., 35 weeks rounded) of the following fiscal year ( i.e., October 1, 2025, to May 31, 2026). We refer to the amount of carryover needed to cover this 35-week period as the continuity set-aside, consistent with the annual OMUFA Financial Reports. 7
Footnotes:
7 ? https://www.fda.gov/about-fda/user-fee-financial-reports/omufa-financial-reports.
To determine the amount of this continuity set-aside, the Agency starts with the additional direct cost adjusted fee revenue of $36,467,438 (calculated in section D), divides it by 52 to yield a weekly operating amount of $701,297, and then multiplies the weekly operating amount by 35. Based on this calculation, FDA requires $24,545,391 to support the program until the FY 2026 facility fees are due. After running analyses on the projected collections and obligations for FY 2025, including accounting for possible financial risks described above, FDA estimates the FY 2025 carryover to be $28,026,448 which is $3,481,057 above the continuity set-aside amount needed to support the program through the 35-week period until the FY 2026 facility fees are due.
To determine whether the carryover above this continuity set-aside is within the 10-week limit for the operating reserve, FDA multiplies the weekly operating amount ($701,297) by 10, resulting in an operating reserve limit of $7,012,969. Because the estimated FY 2025 carryover above the continuity set-aside is below the 10-week threshold, FDA will not increase or reduce the FY 2025 fees or fee revenue under the statutory provision for an operating reserve adjustment. The final FY 2025 OMUFA target facility fee revenue is $36,467,000 (rounded to the nearest thousand dollars).
III. Facility Fee Calculations
A. Facility Fee Revenues and Fees
For FY 2025, facility fee rates are being established to generate a total target revenue amount, as determined under the statute, equal to $36,467,000 (rounded to the nearest thousand dollars). FDA used the methodology described below to determine the appropriate number of MDF and CMO facilities to be used in setting the OMUFA facility fees for FY 2025. FDA took into consideration that the CMO facility fee is equal to two-thirds of the amount of the MDF facility fee (see section 744M(a)(1)(B)(ii) of the FD&C Act).
B. Calculating the Number of Qualifying Facilities and Setting the Facility Fees
[top] For FY 2025, FDA utilized data consisting of the number of facilities that were registered in FDA's eDRLS to manufacture human OTC drug products produced under a monograph? 8 during
Footnotes:
8 ?See section 744M(d) of the FD&C Act. OTC monograph drug facilities had selected in the eDRLS the business operation qualifiers of "manufactures human over-the-counter drug products produced under a monograph" or "contract manufacturing for human over-the-counter drug products produced under a monograph" and indicated at least one of the following business operations: finished dosage form manufacture, label, manufacture, pack, relabel, or repack.
9 ?FDA considers relabelers and repackagers to be a category of OTC monograph drug facilities subject to OMUFA facility fees. See section 744L(10)(A); see also section 744L(10)(A)(iii) of the FD&C Act, excluding from the definition of "OTC monograph drug facility" those facilities whose manufacturing or processing consists solely of a narrow range of specified activities ( e.g., placement of outer overpackaging on products already in final packaged form); cf section 744A(6)(A)(ii) of the FD&C Act (which expressly excludes from the definition of "facility", for purposes of Generic Drug User Fee Amendments facility fees, a business or other entity whose only manufacturing or processing activities are repackaging, relabeling, or testing). See also 21 CFR 207.1 (addressing drug establishment registration), stating that "[m]anufacture means each step in the manufacture, preparation, propagation, compounding, or processing of a drug," and indicating that "the term `manufacture, preparation, propagation, compounding, or processing,' as used in section 510 of the Federal Food, Drug, and Cosmetic Act, includes relabeling, repackaging, and salvaging activities."
Those facilities that only manufacture the active pharmaceutical ingredient of an OTC monograph drug do not meet the definition of an OTC monograph drug facility (see section 744L(10)(A)(i)(II)) of the FD&C Act). Likewise, a facility is not an OTC monograph drug facility if its only manufacturing or processing activities are one or more of the following: (1) production of clinical research supplies; (2) testing; or (3) placement of outer packaging on packages containing multiple products, for such purposes as creating multipacks, when each monograph drug product contained within the overpackaging is already in a final packaged form prior to placement in the outer overpackaging (see section 744L(10)(A)(iii) of the FD&C Act).
Consistent with the January 12, 2021 HHS Federal Register notice? 10 (HHS FRN) and FDA's subsequent Federal Register notices published on March 26, 2021, March 16, 2022, March 27, 2023, and March 29, 2024, announcing the FY 2021, FY 2022, FY 2023, and FY 2024 OMUFA fees (respectively), 11?12?13?14 facilities are not identified as an "OTC monograph drug facility" and will not be assessed a FY 2025 OMUFA facility fee if they: (1) were not registered with FDA as OTC drug manufacturers prior to the HHS declaration of the COVID-19 public health emergency (PHE) on January 27, 2020;? 15 (2) registered with FDA on or after the declaration of the COVID-19 PHE on January 27, 2020; (3) registered for the sole purpose of producing hand sanitizer products during the COVID-19 PHE; and (4) ceased manufacturing hand sanitizer products and delisted and deregistered in eDRLS before 12 a.m. Eastern Time on December 31, 2024. We note that under the FD&C Act, whether an entity is subject to OMUFA fees has no bearing on whether the entity or the entity's products are subject to other requirements under the FD&C Act. FDA will continue to use its regulatory compliance and enforcement tools to protect consumers, including from hand sanitizers or other drugs that are potentially dangerous or subpotent.
Footnotes:
10 ?See 86 FR 2420, https://www.federalregister.gov/documents/2021/01/12/2021-00237/notice-that-persons-that-entered-the-over-the-counter-drug-market-to-supply-hand-sanitizer-during.
11 ?See 86 FR 16223, https://www.federalregister.gov/documents/2021/03/26/2021-06361/fee-rates-under-the-over-the-counter-monograph-drug-user-fee-program-for-fiscal-year-2021.
12 ?See 87 FR 14888, https://www.federalregister.gov/documents/2022/03/16/2022-05542/over-the-counter-monograph-drug-user-fee-rates-for-fiscal-year-2022.
13 ?See 88 FR 18156, https://www.federalregister.gov/documents/2023/03/27/2023-06299/over-the-counter-monograph-drug-user-fee-rates-for-fiscal-year-2023.
14 ?See 88 FR 22156, https://www.federalregister.gov/documents/2024/03/29/2024-06723/over-the-counter-monograph-drug-user-fee-program-facility-fee-rates-for-fiscal-year-2024.
15 ?See https://aspr.hhs.gov/legal/PHE/Pages/2019-nCoV.aspx#:~:text=As%20a%20result%20of%20confirmed,January%2027%2C%202020%2C%20nationwide.
The January 12, 2021 HHS FRN explains that "[t]he Department's conclusion [that certain hand sanitizer manufacturers are not identified as OTC monograph drug facilities] does not apply to such persons which (1) manufacture, distribute, and sell over-the-counter drugs in addition to hand sanitizer or (2) continue to manufacture (as opposed to hold, distribute, or sell existing inventories) hand sanitizer products as of December 31 of the year immediately following the year during which the COVID-19 Public Health Emergency is terminated. In those cases, the Department may identify such persons as OTC drug manufacturing facilities" ? 16 (emphasis added). Accordingly, as the PHE expired on May 11, 2023, those facilities which "continue to manufacture" solely hand sanitizer products as of December 31, 2024, are identified as OTC monograph drug facilities and are subject to an OMUFA facility fee for FY 2025. Conversely, if such facilities ceased manufacturing hand sanitizer products and delisted and deregistered to reflect that before 12 a.m. Eastern Time on December 31, 2024, they are not identified as an OTC monograph drug facility? 17 and would not be considered fee liable for purposes of FY 2025 OMUFA facility fees. 18 FDA communicated this deadline to stakeholders on multiple occasions, including in the FY 2024 OMUFA Facility Fee FRN, 19 presentations to industry, and OMUFA listserv emails.
Footnotes:
16 ?See https://www.federalregister.gov/documents/2021/01/12/2021-00237/notice-that-persons-that-entered-the-over-the-counter-drug-market-to-supply-hand-sanitizer-during.
17 ?Id.
18 ?Id.
19 ?Available at https://www.federalregister.gov/documents/2024/03/29/2024-06723/over-the-counter-monograph-drug-user-fee-program-facility-fee-rates-for-fiscal-year-2024.
[top] In undertaking the statutorily directed fee calculations for FY 2024 fees, the Agency also made certain assumptions, including that: (1) facilities using expired Structured Product Labeling codes in eDRLS, that have not reregistered, were no longer manufacturing and marketing OTC monograph drugs; (2) facilities that have deregistered in eDRLS have exited the market; (3) facilities that FDA believes registered incorrectly as OTC monograph drug facilities (for example, because the associated drug listings for these facilities did not include OTC monograph drugs but instead indicated such products as OTC drug products under an approved drug application or OTC animal drug products) were not engaged in manufacturing or processing
In addition, the Agency made certain assumptions with respect to hand sanitizer manufacturers that remained registered after 12 a.m. Eastern Time on December 31, 2024, including that: (1) hand sanitizer manufactures that have deregistered in eDRLS after December 31, 2024, have exited the market; (2) hand sanitizer manufacturers that did not actively update their registration in eDRLS during the FY 2025 fee liable period and let their registration lapse have likely exited the market; and (3) for the remaining hand sanitizer manufacturers that are newly fee liable, FDA estimated a portion will be in arrears based on a review of the prior 3-year average for newly registered facilities in arrears.
Based on the above-referenced factors and assumptions, FDA estimates there will be 1,134 OMUFA fee-paying units. The Agency estimates that 57 percent (1,134 × 0.57 = 646, rounded) will incur the MDF fee and 43 percent (1,134 × 0.43 = 488, rounded) will incur the CMO fee.
To determine the number of full fee-paying equivalents (the denominator) to be used in setting the OMUFA fees, FDA assigns a value of 1 to each MDF (646) and a value of 2⁄3 to each CMO (488 × 2/3 = 325) for a full facility equivalent of 971 (rounded). The target fee revenue of $36,467,000 is then divided by 971 for an MDF fee of $37,556 and a CMO fee of $25,037.
IV. Fee Schedule for FY 2025
The fee rates for FY 2025 are displayed in table 4.
| Fee category | FY 2025 fee rates |
|---|---|
| MDF | $37,556 |
| CMO | 25,037 |
V. Fee Payment Options and Procedures
The new facility fee rates are for the period from October 1, 2024, through September 30, 2025. To pay the MDF and CMO fees, complete an OTC Monograph User Fee Cover Sheet, available at: https://userfees.fda.gov/OA_HTML/omufaCAcdLogin.jsp.
A user fee identification (ID) number will be generated. Payment must be made in U.S. currency by electronic check or wire transfer, payable to the order of the Food and Drug Administration. The preferred payment method is online using electronic check (Automated Clearing House (ACH) also known as eCheck).
FDA has partnered with the U.S. Department of the Treasury to use Pay.gov, a web-based payment application, for online electronic payment. The Pay.gov feature is available on the FDA website after completing the OTC Monograph User Fee Cover Sheet and generating the user fee ID number. Secure electronic payments can be submitted using the User Fees Payment Portal at https://userfees.fda.gov/pay. (Note: Only full payments are accepted through https://userfees.fda.gov/pay. No partial payments can be made online). Once an invoice is located, "Pay Now" should be selected to be redirected to Pay.gov. Electronic payment options are based on the balance due. 20
Footnotes:
20 ?Payment by credit card is available for balances that are less than $25,000 (Discover, VISA, MasterCard, American Express). If the balance exceeds this amount, only the ACH option is available. Payments must be made using U.S. bank accounts as well as U.S. credit cards.
For payments made by wire transfer, include the unique user fee ID number to ensure that the payment is applied to the correct fee(s). Without the unique user fee ID number, the payment may not be applied, which could result in consequences of nonpayment per section 744M(e)(1) of the FD&C Act. The originating financial institution may charge a wire transfer fee. Applicable wire transfer fees must be included with payment to ensure fees are fully paid. Questions about wire transfer fees should be addressed to the financial institution. The account information for wire transfers is as follows: U.S. Department of the Treasury, TREAS NYC, 33 Liberty St., New York, NY 10045, Acct. No.: 75060099, Routing No.: 021030004, SWIFT: FRNYUS33. If needed, FDA's tax identification number is 53-0196965.
If you are assessed an FY 2025 OMUFA facility fee and believe your facility is not an OTC monograph drug facility as described in this notice, please contact CDERCollections@fda.hhs.gov.
Dated: March 18, 2025.
P. Ritu Nalubola,
Associate Commissioner for Policy.
[FR Doc. 2025-04860 Filed 3-20-25; 8:45 am]
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