Metformin Hydrochloride
- Product NDC
- 71335-9752
- 11-digit product format
- 713359752
- Labeler code
- 71335
- Product ID
- 71335-9752_11d52559-bfde-4c2a-9602-f18fb3187617
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077078
- Marketing category
- ANDA
- Marketing start
- 2019-03-15
- 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 |
|---|
| 71335-9752-1 | 71335975201 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9752-1) | 2024-04-05 | No | No | Historical |
| 71335-9752-2 | 71335975202 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9752-2) | 2024-04-05 | No | No | Historical |
| 71335-9752-3 | 71335975203 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9752-3) | 2024-04-05 | No | No | Historical |
| 71335-9752-4 | 71335975204 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9752-4) | 2024-04-05 | No | No | Historical |
| 71335-9752-5 | 71335975205 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9752-5) | 2023-07-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metformin Hydrochloride | Bryant Ranch Prepack | 2024-04-05 | HUMAN PRESCRIPTION DRUG LABEL | 101 |