METFORMIN HYDROCHLORIDE
- Product NDC
- 62207-496
- 11-digit product format
- 622070496
- Labeler code
- 62207
- Product ID
- 62207-496_414662c8-b86d-4c80-e063-6294a90a3cb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Granules India Ltd
- Application
- ANDA213344
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 62207-496-47 | 62207049647 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-496-47) | 2021-02-01 | No | No | Historical |
| 62207-496-54 | 62207049654 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-496-54) | 2021-02-01 | No | No | Historical |