METFORMIN HYDROCHLORIDE
- Product NDC
- 63629-8504
- 11-digit product format
- 636298504
- Labeler code
- 63629
- Product ID
- 63629-8504_5c1f7ec4-ea5a-4745-b159-3113906e0611
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203769
- Marketing category
- ANDA
- Marketing start
- 2015-02-01
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-8504-1 | 63629850401 | 100 TABLET in 1 BOTTLE (63629-8504-1) | 100 tablet | 2021-05-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | Bryant Ranch Prepack | 2023-03-28 | HUMAN PRESCRIPTION DRUG LABEL | 102 |