NDC 73377-016 - Ranitidine HCL
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
- 73377-016
- Package NDCs from labels
- 73377-016-01, 73377-016-02
- Manufacturer
- AX Pharmaceutical Corp
- Effective date
- 2020-02-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ranitidine HCL - AX Pharmaceutical Corp | AX Pharmaceutical Corp | 2020-02-11 | BULK INGREDIENT |
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 |
|---|---|---|---|---|---|---|
| Ranitidine | RANITIDINE | Amneal Pharmaceuticals of New York LLC | b38a3332-5c54-453f-aeb7-070f830955c2 | 2026-05-01 | Adverse reactions | BK76465IHM |
| RANITIDINE | RANITIDINE | Rising Pharma Holdings, Inc. | 0fba6615-37c2-4ba6-b6e5-09599369a5bc | 2025-12-05 | Adverse reactions | BK76465IHM |
| Ranitidine | RANITIDINE | Dr. Reddy's Laboratories Limited | 12a38e29-130c-6d41-1753-acccb0b41efe | 2025-05-23 | Warnings | BK76465IHM |
| Ranitidine | RANITIDINE | Dr. Reddy's Laboratories Limited | 00df8a42-296f-80dd-98af-ee8b30eb38cc | 2025-05-23 | Warnings | BK76465IHM |
| Ranitidine | RANITIDINE | Ajanta Pharma USA Inc. | fb67e8c7-b817-4253-a1a1-5ecdcee694cf | 2021-11-24 | Adverse reactions | BK76465IHM |
| Ranitidine Hydrochloride | RANITIDINE HYDROCHLORIDE | Dr. Reddy's Laboratories Limited | 7bf94bf7-fa11-70be-9f65-fe26a3db5a63 | 2018-11-21 | Adverse reactions | BK76465IHM |
| Acid Reducer | RANITIDINE HYDROCHLORIDE | WinCo Foods, LLC | 70bc7062-ab3c-43eb-b524-0d8c6d1a674d | 2014-12-10 | Warnings | BK76465IHM |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.