METFORMIN HYDROCHLORIDE
- Product NDC
- 70436-052
- 11-digit product format
- 704360052
- Labeler code
- 70436
- Product ID
- 70436-052_98652764-5aba-7272-e053-2995a90a285a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Slate Run Pharmaceuticals, LLC
- Application
- ANDA211052
- Marketing category
- ANDA
- Marketing start
- 2020-06-06
- 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