METFORMIN HYDROCHLORIDE
- Product NDC
- 73317-4256
- 11-digit product format
- 733174256
- Labeler code
- 73317
- Product ID
- 73317-4256_da8b7f65-defe-4129-9895-e862dfa1df92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- SLV PHARMACEUTICALS LLC DBA AUM PHARMACEUTICALS
- Application
- ANDA213334
- Marketing category
- ANDA
- Marketing start
- 2021-04-16
- 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
- 2022-12-31
- 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 |
|---|
| 73317-4256-1 | 73317425601 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (73317-4256-1) | 2021-04-28 | 0000-00-00 | No | No | Current |