METFORMIN HYDROCHLORIDE
- Product NDC
- 63629-9147
- 11-digit product format
- 636299147
- Labeler code
- 63629
- Product ID
- 63629-9147_f70200e9-9e16-40ee-a09f-04a418ae1d36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076756
- Marketing category
- ANDA
- Marketing start
- 2020-08-06
- 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 |
|---|
| 63629-9147-1 | 63629914701 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9147-1) | 2022-01-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | Bryant Ranch Prepack | 2023-02-23 | HUMAN PRESCRIPTION DRUG LABEL | 102 |