METFORMIN HYDROCHLORIDE
- Product NDC
- 72162-1522
- 11-digit product format
- 721621522
- Labeler code
- 72162
- Product ID
- 72162-1522_46e0a696-b726-4315-8b2d-04c4a6deae29
- 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
- 500 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 |
|---|
| 72162-1522-1 | 72162152201 | 100 TABLET in 1 BOTTLE (72162-1522-1) | 100 tablet | 2024-02-05 | No | No | Historical |
| 72162-1522-5 | 72162152205 | 500 TABLET in 1 BOTTLE (72162-1522-5) | 500 tablet | 2024-02-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METFORMIN HYDROCHLORIDE | Bryant Ranch Prepack | 2024-02-05 | HUMAN PRESCRIPTION DRUG LABEL | 100 |