METFORMIN HYDROCHLORIDE
- Product NDC
- 70518-1606
- 11-digit product format
- 705181606
- Labeler code
- 70518
- Product ID
- 70518-1606_e5820c12-90d9-1d0d-e053-2a95a90a056e
- 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
- 2018-10-29
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1606-2 | 70518160602 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1606-2) | | 2018-11-26 | 0000-00-00 | No | No | Current |
| 70518-1606-4 | 70518160604 | 360 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1606-4) | | 2019-05-02 | 0000-00-00 | No | No | Current |
| 70518-1606-5 | 70518160605 | 100 POUCH in 1 BOX (70518-1606-5) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-1606-6) | 100 pouch | 2020-06-26 | 0000-00-00 | No | No | Current |
| 70518-1606-7 | 70518160607 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1606-7) | | 2020-07-07 | 0000-00-00 | No | No | Current |
| 70518-1606-8 | 70518160608 | 100 POUCH in 1 BOX (70518-1606-8) > 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-1606-9) | 100 pouch | 2020-09-11 | 0000-00-00 | No | No | Current |