METFORMIN HYDROCHLORIDE
- Product NDC
- 71610-923
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA203769
- Marketing category
- ANDA
- Substance
- METFORMIN HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-923-30 | 30 TABLET in 1 BOTTLE (71610-923-30) | 2025-07-08 | | No | Historical |
| 71610-923-53 | 60 TABLET in 1 BOTTLE (71610-923-53) | 2025-07-08 | | No | Historical |
| 71610-923-60 | 90 TABLET in 1 BOTTLE (71610-923-60) | 2025-07-08 | | No | Historical |
| 71610-923-80 | 180 TABLET in 1 BOTTLE (71610-923-80) | 2025-07-08 | | No | Historical |
| 71610-923-92 | 270 TABLET in 1 BOTTLE (71610-923-92) | 2025-07-08 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | Aphena Pharma Solutions - Tennessee, LLC | 2025-07-09 | HUMAN PRESCRIPTION DRUG LABEL | 1 |