METFORMIN HYDROCHLORIDE
- Product NDC
- 50090-7577
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA217631
- Marketing category
- ANDA
- Substance
- METFORMIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7577-0 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7577-0) | 2025-06-09 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | A-S Medication Solutions | 2025-06-11 | Human Prescription Drug Label | 1 |