Metformin Hydrochloride

Product NDC
50090-7013
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metformin Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090564
Marketing category
ANDA
Substance
METFORMIN HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7013-0100 BLISTER PACK in 1 CARTON (50090-7013-0) / 1 TABLET in 1 BLISTER PACK2024-01-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideA-S Medication Solutions2024-01-08HUMAN PRESCRIPTION DRUG LABEL1