Metformin hydrochloride
- Product NDC
- 68645-546
- 11-digit product format
- 686450546
- Labeler code
- 68645
- Product ID
- 68645-546_7a175761-fb19-471e-ab75-f6801306680e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Legacy Pharmaceutical Packaging, LLC
- Application
- ANDA090564
- Marketing category
- ANDA
- Marketing start
- 2014-07-16
- Marketing end
- 2021-10-31
- Substance
- METFORMIN HYDROCHLORIDE
- Active strength
- 1000 mg/1
- Pharmacologic classes
- Biguanide [EPC],Biguanides [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 68645-546-59 | 68645054659 | 60 TABLET, FILM COATED in 1 BOTTLE (68645-546-59) | 2014-07-16 | 2021-10-31 | No | No | Current |