METFORMIN HYDROCHLORIDE

Product NDC
50090-7918
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
METFORMIN HYDROCHLORIDE
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA217631
Marketing category
ANDA
Substance
METFORMIN HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7918-090 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7918-0) 2026-02-26NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
METFORMIN HYDROCHLORIDEA-S Medication Solutions2026-03-03Human Prescription Drug Label1