NDC 51662-1375-01 - 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
- 51662-1375
- Requested NDC
- 51662-1375-01
- Package NDCs from labels
- 51662-1375-1, 51662-1375-2, 51662-1375-01
- Manufacturer
- HF Acquisition Co LLC, DBA HealthFirst
- Effective date
- 2022-10-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| FAMOTIDINE - HF Acquisition Co LLC, DBA HealthFirst | HF Acquisition Co LLC, DBA HealthFirst | 2022-10-01 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51662-1375-1 | FAMOTIDINE | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 2 | 3 | |
| 51662-1375-2 | FAMOTIDINE | 1 in 1 POUCH | INJECTION, SOLUTION | 1 | 3 | |
| 51662-1375-2 | FAMOTIDINE | 2 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 2 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51662-1375 | FAMOTIDINE INJECTION, SOLUTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST] | 3 | Current NDC, Legacy NDC, 3 package rows | 20221002_9948991d-9405-c7c8-e053-2995a90a60ca.zip |
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 | BluePoint Laboratories | 8c7ca3cc-ff90-42a7-9218-554cf15348a3 | 2021-04-13 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Dr.Reddy's Laboratories Limited | 06d286ce-14b3-4b66-8b42-ac4a10a0fc90 | 2020-11-17 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Aphena Pharma Solutions - Tennessee, LLC | b1839d23-20f4-4651-a7d2-8bc3a7583917 | 2020-07-06 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| Famotidine | FAMOTIDINE | Proficient Rx LP | 1e2003d4-09a3-4cc8-af3d-93d29b9123c0 | 2020-07-01 | Warnings, Adverse reactions | 5QZO15J2Z8 |
| 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 |
| Famotidine | FAMOTIDINE | Lupin Pharmaceuticals,Inc. | a0bdf4d1-8458-4e4f-95aa-bcc38c0f32f8 | 2017-11-21 | Adverse reactions | 5QZO15J2Z8 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.