Metformin Hydrochloride

Product NDC
50090-7595
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
50090-7595-060 TABLET in 1 BOTTLE (50090-7595-0) 2025-07-07NoHistorical
50090-7595-3100 TABLET in 1 BOTTLE (50090-7595-3) 2025-07-07NoHistorical
50090-7595-430 TABLET in 1 BOTTLE (50090-7595-4) 2025-07-07NoHistorical
50090-7595-5180 TABLET in 1 BOTTLE (50090-7595-5) 2025-07-07NoHistorical
50090-7595-690 TABLET in 1 BOTTLE (50090-7595-6) 2025-07-07NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Metformin HydrochlorideA-S Medication Solutions2025-07-09HUMAN PRESCRIPTION DRUG LABEL1