NDC 71872-7366-01 - 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
- 71872-7366
- Requested NDC
- 71872-7366-01
- Package NDCs from labels
- 71872-7366-1, 71872-7366-01
- Manufacturer
- Medical Purchasing Solutions, LLC
- Effective date
- 2026-04-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Famotidine - Medical Purchasing Solutions, LLC | Medical Purchasing Solutions, LLC | 2026-04-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71872-7366-1 | Famotidine | 1 in 1 BAG | INJECTION, SOLUTION | 1 | 1 | |
| 71872-7366-1 | Famotidine | 2 mL in 1 VIAL | INJECTION, SOLUTION | 2 | 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 | Proficient Rx LP | 92048836-e692-4ce1-93f4-88b00acabcde | 2019-11-01 | Adverse reactions | 5QZO15J2Z8 |
| heartburn relief original strength | FAMOTIDINE | Proficient Rx LP | 5567aaaf-b4f2-4604-b841-c9447e77256c | 2019-10-01 | Warnings | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Teva Pharmaceuticals USA, Inc. | 4c6f4f9e-f3f5-4ecf-9f40-887e037e8847 | 2019-01-01 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Dynamic Eyewash with Eyecup | WATER | Dynamic Safety International | 7d3af0f4-0e1f-9ea5-e053-2991aa0af7a2 | 2018-12-17 | Warnings | 059QF0KO0R |
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| Famotidine | FAMOTIDINE | Lupin Pharmaceuticals,Inc. | a0bdf4d1-8458-4e4f-95aa-bcc38c0f32f8 | 2017-11-21 | Adverse reactions | 5QZO15J2Z8 |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.