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 |
|---|---|---|---|---|---|---|
| DECONIMO Reconstitution | DECONIMO RECONSTITUTION | Image Amazon LLC | 57ab9b1c-9a18-3786-e063-6394a90a2c63 | 2026-07-28 | Warnings | 059QF0KO0R |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Ascend Laboratories, LLC | 4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | 5QZO15J2Z8 |
| DUAL ACTION COMPLETE | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | Amazon.com Services LLC | 4e8a936c-b876-4923-ad9e-d23537b5d7cf | 2026-07-28 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Ascend Laboratories, LLC | b2228be0-472b-4e47-9910-af0bf12fde77 | 2026-07-27 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Kenvue Brands LLC | a2ef8424-7d80-42b0-a01e-f378f629b2b6 | 2026-07-24 | Warnings | 5QZO15J2Z8 |
| Lidocaine Plus Pain Relieving | LIDOCAINE HYDROCHLORIDE, BENZYL ALCOHOL | CVS Pharmacy | 49003aac-184c-ae33-e063-6294a90a29c0 | 2026-07-24 | Warnings | LKG8494WBH |
| COMPLETE ACID REDUCER | FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 962ced24-0fb3-4aba-b32e-2e6fa1c1c5d7 | 2026-07-22 | Warnings | 5QZO15J2Z8 |
| Sterile Water | WATER | Cardinal Health 107, LLC | 9655cd02-82b5-4a75-813b-854b19551481 | 2026-07-21 | Warnings, Adverse reactions | 059QF0KO0R |
| Curist Acid Relief | FAMOTIDINE 20 MG | Little Pharma, Inc. | 0fdfcc7c-aeed-6bd0-e063-6394a90ae52d | 2026-07-16 | Warnings | 5QZO15J2Z8 |
| FAMOTIDINE | FAMOTIDINE | HAWAII REPACK, INC. | eec89230-47fc-4139-a370-b4f9e225e8c0 | 2026-07-13 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Advanced Rx of Tennessee, LLC | 5648ca13-1add-56ec-e063-6294a90a6f29 | 2026-07-10 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Dr. Drop NMN Vital Balance (Drop No.1 Cream 90g) | NMN (NICOTINAMIDE MONONUCLEOTIDE), ECTOIN (ECTOINE) | Reedfresh Co., LTD | 55d703ca-ff9d-0dbc-e063-6294a90ab6b1 | 2026-07-05 | Warnings | 059QF0KO0R |
| Pepcid Complete | FAMOTIDINE, CALCIUM CARBONATE, AND MAGNESIUM HYDROXIDE | Select Consumer Group | 55cc3304-9094-3da8-e063-6394a90aa49b | 2026-07-04 | Warnings | 5QZO15J2Z8 |
| Eyesaline Eyewash Concentrate | PURIFIED WATER | Protective Industrial Products, Inc. | 558e5926-9027-d3f6-e063-6294a90ab121 | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 2000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a1d07e-0006-0c75-e063-6394a90a7acc | 2026-07-02 | Warnings | 059QF0KO0R |
| Fendall 1000 Pure Flow | PURIFIED WATER | Protective Industrial Products, Inc. | 55a2f4da-bb1e-8ead-e063-6394a90af72e | 2026-07-02 | Warnings | 059QF0KO0R |
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| CareOne Acid Relief | FAMOTIDINE | American Sales Company | ed474c9d-c08b-4f52-8b24-5887978e4275 | 2026-07-01 | Warnings | 5QZO15J2Z8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.