Metformin
- Product NDC
- 50090-7373
- 11-digit product format
- 500907373
- Labeler code
- 50090
- Product ID
- 50090-7373_c15c8d87-d12e-4e61-b5b1-d8c764b5c48a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin ER 750 mg
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209313
- Marketing category
- ANDA
- Marketing start
- 2018-07-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 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 |
|---|
| 50090-7373-0 | 50090737300 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7373-0) | 2024-10-18 | No | No | Historical |