METFORMIN HYDROCHLORIDE
- Product NDC
- 70518-3200
- 11-digit product format
- 705183200
- Labeler code
- 70518
- Product ID
- 70518-3200_ebf23241-ec48-7abe-e053-2a95a90a1e3d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2021-08-26
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Biguanide [EPC], Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3200-0 | 70518320000 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3200-0) | 2021-08-26 | 0000-00-00 | No | No | Current |