METFORMIN HYDROCHLORIDE
- Product NDC
- 70518-3260
- 11-digit product format
- 705183260
- Labeler code
- 70518
- Product ID
- 70518-3260_e81667c7-f32f-bb30-e053-2995a90ae4fd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA201991
- Marketing category
- ANDA
- Marketing start
- 2021-10-30
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 500 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3260-0 | 70518326000 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3260-0) | 2021-10-30 | 0000-00-00 | No | No | Current |
| 70518-3260-1 | 70518326001 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3260-1) | 2022-09-03 | 0000-00-00 | No | No | Current |