Metformin Hydrochloride
- Product NDC
- 50090-7107
- 11-digit product format
- 500907107
- Labeler code
- 50090
- Product ID
- 50090-7107_5ee76af1-a448-4d44-96d1-a8c914e611a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209882
- Marketing category
- ANDA
- Marketing start
- 2021-05-17
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 850 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 786Z46389E | METFORMIN HYDROCHLORIDE | 1115-70-4 | METFORMIN HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7107-0 | 50090710700 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7107-0) | 2024-03-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | A-S Medication Solutions | 2024-03-10 | Human Prescription Drug Label | 1 |