METFORMIN HYDROCHLORIDE
- Product NDC
- 55700-320
- 11-digit product format
- 557000320
- Labeler code
- 55700
- Product ID
- 55700-320_16c6d77e-ca53-4422-b0f9-5a9c2ab496c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2006-02-09
- 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#