metformin hydrochloride
- Product NDC
- 24979-146
- 11-digit product format
- 249790146
- Labeler code
- 24979
- Product ID
- 24979-146_c0cebca5-937a-4659-a07e-7e9dadf20584
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metformin hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- TWi Pharmaceuticals, Inc.
- Application
- ANDA213247
- Marketing category
- ANDA
- Marketing start
- 2021-11-01
- Marketing end
- 0000-00-00
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 24979-146-04 | 24979014604 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-146-04) | 2021-11-01 | 0000-00-00 | No | No | Current |
| 24979-146-40 | 24979014640 | 750 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (24979-146-40) | 2021-11-01 | 0000-00-00 | No | No | Current |