Metformin Hydrochloride

Product NDC
50090-7010
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
50090-7010-060 TABLET in 1 BOTTLE (50090-7010-0) 2024-01-04NoHistorical
50090-7010-3100 TABLET in 1 BOTTLE (50090-7010-3) 2024-01-04NoHistorical
50090-7010-430 TABLET in 1 BOTTLE (50090-7010-4) 2024-01-04NoHistorical
50090-7010-5180 TABLET in 1 BOTTLE (50090-7010-5) 2024-01-04NoHistorical
50090-7010-690 TABLET in 1 BOTTLE (50090-7010-6) 2024-01-04NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideA-S Medication Solutions2024-01-18HUMAN PRESCRIPTION DRUG LABEL1