Metformin Hydrochloride
- Product NDC
- 68788-8652
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090564
- Marketing category
- ANDA
- Substance
- METFORMIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-8652-1 | 100 TABLET in 1 BOTTLE (68788-8652-1) | 2024-05-03 | | No | Historical |
| 68788-8652-3 | 30 TABLET in 1 BOTTLE (68788-8652-3) | 2024-05-03 | | No | Historical |
| 68788-8652-6 | 60 TABLET in 1 BOTTLE (68788-8652-6) | 2024-05-03 | | No | Historical |
| 68788-8652-7 | 180 TABLET in 1 BOTTLE (68788-8652-7) | 2024-05-03 | | No | Historical |
| 68788-8652-8 | 120 TABLET in 1 BOTTLE (68788-8652-8) | 2024-05-03 | | No | Historical |
| 68788-8652-9 | 90 TABLET in 1 BOTTLE (68788-8652-9) | 2024-05-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | Preferred Pharmaceuticals Inc. | 2025-08-06 | HUMAN PRESCRIPTION DRUG LABEL | 2 |