METFORMIN HYDROCHLORIDE
- Product NDC
- 63739-640
- 11-digit product format
- 637390640
- Labeler code
- 63739
- Product ID
- 63739-640_eca6f8a3-5b07-4174-9904-6f3105425c45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metformin Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA077880
- Marketing category
- ANDA
- Marketing start
- 2012-12-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#