METFORMIN HYDROCHLORIDE
- Product NDC
- 70914-000
- 11-digit product format
- 709140000
- Labeler code
- 70914
- Product ID
- 70914-000_fb74b13b-94b7-475e-b45b-7065f29e9a1f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METFORMIN HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Hudson Scientific LLC
- Application
- ANDA077336
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record