METFORMIN HYDROCHLORIDE
- Product NDC
- 72789-455
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA201991
- Marketing category
- ANDA
- Substance
- METFORMIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72789-455-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-455-30) | 2024-12-05 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | PD-Rx Pharmaceuticals, Inc. | 2025-08-22 | HUMAN PRESCRIPTION DRUG LABEL | 7 |