NDC 0641-6021-01 - Famotidine
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0641-6021
- Requested NDC
- 0641-6021-01
- Package NDCs from labels
- 0641-6021-01, 0641-6021-10
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Effective date
- 2024-04-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Famotidine Injection, USP | Hikma Pharmaceuticals USA Inc. | 2024-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2013-02-13 | Indexing - Billing Unit |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0641-6021-01 | Famotidine | 20 mL in 1 VIAL | INJECTION | 20 | 9 | |
| 0641-6021-10 | Famotidine | 10 in 1 CARTON | INJECTION | 10 | 9 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0641-6021-01 | ML - Milliliter | 0641-6021 | 613a20d9-c98f-4731-9be1-7db259da9087 | 1 | 2013-02-13 |
| 0641-6021-10 | ML - Milliliter | 0641-6021 | 6ed8396c-a368-4580-9b5c-58077e01468d | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| FAMOTIDINE | ACTIVE INGREDIENT | 5QZO15J2Z8 | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 | |
| FAMOTIDINE | ACTIVE MOIETY | 5QZO15J2Z8 | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 | |
| ASPARTIC ACID | INACTIVE INGREDIENT | 30KYC7MIAI | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 | |
| BENZYL ALCOHOL | INACTIVE INGREDIENT | LKG8494WBH | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 | |
| MANNITOL | INACTIVE INGREDIENT | 3OWL53L36A | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | FAMOTIDINE INJECTION [WEST-WARD PHARMACEUTICAL CORP.] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Famotidine | FAMOTIDINE | REMEDYREPACK INC. | 669fbd46-cae5-4477-884e-8eca893d2e05 | 2026-09-09 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| COMPLETE ACID REDUCER | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | b023cd92-eabb-474b-9b5a-4b46cf48256b | 2026-09-08 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Aurohealth LLC | 5b161f25-c578-4ff4-a931-ff3a1e681c50 | 2026-09-04 | Warnings | 5QZO15J2Z8 |
| ACID REDUCER | FAMOTIDINE | Amazon.com Services LLC | d5823283-aa97-451e-ba0d-69f0e79c8514 | 2026-08-31 | Warnings | 5QZO15J2Z8 |
| FAMOTIDINE | FAMOTIDINE | REMEDYREPACK INC. | 9c5dce17-1865-4aa6-89f6-24dd55b5f06c | 2026-08-27 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| KUGIG ALOE FOAMING INTIMATE WASH | INTIMATE CLEANSING FOAM | Hong Kong KangXing Centennial Management Limited | 59f4d398-1186-a168-e063-6294a90ab44b | 2026-08-26 | Warnings | 059QF0KO0R |
| Pepcid Complete Dual Action Berry Flavor | FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | Jones Healthcare Group - Packaging Services, Inc | fff07b68-02ca-438e-8d53-5b4edf5eefc5 | 2026-08-25 | Warnings | 5QZO15J2Z8 |
| Sterile Water | WATER | REMEDYREPACK INC. | 5dd5d148-6e23-41de-bff5-551b2aea9598 | 2026-08-24 | Warnings, Adverse reactions | 059QF0KO0R |
| Famotidine | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 599642c8-51cd-4220-e063-6394a90a5e20 | 2026-08-24 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| 0.9% Benzyl Alcohol Solution (Laboratory Use Only) | 0.9% BENZYL ALCOHOL SOLUTION (LABORATORY USE ONLY) | Guangzhou Huanmei Cosmetics Co., Ltd | 5976bde6-0999-ffc4-e063-6394a90aadcf | 2026-08-20 | Warnings | LKG8494WBH |
| Famotidine | FAMOTIDINE | Major Pharmaceuticals | 3e6d167f-91e4-4122-911d-d3da66386f44 | 2026-08-20 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| TrophAmine | ISOLEUCINE, LEUCINE, LYSINE ACETATE, METHIONINE, PHENYLALANINE, THREONINE, TRYPTOPHAN, VALINE, CYSTEINE HYDROCHLORIDE, HISTIDINE, TYROSINE, N-ACETYL-TYROSINE, ALANINE, ARGININE, PROLINE, SERINE, GLYCINE, ASPARTIC ACID, GLUTAMIC ACID, AND TAURINE | B. Braun Medical Inc. | cb6d23ff-3ec5-445a-acbe-f88fd57949bf | 2026-08-19 | Warnings, Adverse reactions | 30KYC7MIAI |
| BM BM63 DROPS | CEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADEN | BM Private Limited | 59006d82-610a-2e08-e063-6394a90af1ed | 2026-08-14 | Warnings | 059QF0KO0R |
| Famotidine | FAMOTIDINE | Preferred Pharmaceuticals Inc. | cd95271c-cf39-47fb-97a6-f6ee1e619e4a | 2026-08-12 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| heartburn prevention | FAMOTIDINE | Kroger Company | c97851ef-7b49-4f6c-b165-147555db101a | 2026-08-11 | Warnings | 5QZO15J2Z8 |
| Sterile Water | WATER | Cardinal Health 107, LLC | 48d75a7c-8329-48a8-bea0-a8c144ddf637 | 2026-08-07 | Warnings, Adverse reactions | 059QF0KO0R |
| ACID REDUCER | FAMOTIDINE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | f347f870-1da4-4a77-8c20-63b703d24071 | 2026-08-05 | Warnings | 5QZO15J2Z8 |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Doc Rx | 9f5de6af-e555-4efd-a3ed-b72c34c051b6 | 2026-08-01 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| Garzulys | INSULIN ASPART-FSAN | Meitheal Pharmaceuticals Inc. | 30c64769-d2f7-4604-ac9e-2a6bc09506c9 | 2026-07-31 | Warnings, Adverse reactions | 059QF0KO0R |
| FAMOTIDINE | FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | a0f38398-4d34-4ecc-8a6a-37732adaaad3 | 2026-07-30 | Warnings, Adverse reactions | 5QZO15J2Z8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.