Metformin Hydrochloride
- Product NDC
- 68071-3833
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209882
- Marketing category
- ANDA
- Substance
- METFORMIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3833-8 | 180 TABLET, FILM COATED in 1 BOTTLE (68071-3833-8) | 2025-04-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | NuCare Pharmaceuticals,Inc. | 2025-04-18 | HUMAN PRESCRIPTION DRUG LABEL | 1 |