Metformin Hydrochloride
- Product NDC
- 68071-3212
- 11-digit product format
- 680713212
- Labeler code
- 68071
- Product ID
- 68071-3212_bb144885-fad2-3699-e053-2995a90aa51d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmarmaceuticals, Inc.
- Application
- ANDA077095
- Marketing category
- ANDA
- Marketing start
- 2005-01-14
- 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 |
|---|
| 68071-3212-1 | 68071321201 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-3212-1) | 2017-06-09 | 0000-00-00 | No | No | Current |