FAMOTIDINE
- Product NDC
- 72789-345
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FAMOTIDINE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA215630
- Marketing category
- ANDA
- Substance
- FAMOTIDINE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-345-30 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-345-30) | 2023-08-07 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 4 |
| FAMOTIDINE | PD-Rx Pharmaceuticals, Inc. | 2024-02-19 | HUMAN PRESCRIPTION DRUG LABEL | 3 |