METFORMIN HYDROCHLORIDE EXTENDED RELEASE
- Product NDC
- 70518-2480
- 11-digit product format
- 705182480
- Labeler code
- 70518
- Product ID
- 70518-2480_e6e8d52a-a53a-481a-e053-2995a90a40b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA090295
- Marketing category
- ANDA
- Marketing start
- 2019-12-12
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2480-0 | 70518248000 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2480-0) | | 2019-12-12 | 0000-00-00 | No | No | Current |
| 70518-2480-1 | 70518248001 | 100 POUCH in 1 BOX (70518-2480-1) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2480-2) | 100 pouch | 2021-07-14 | 0000-00-00 | No | No | Current |