Simvastatin

Product NDC
50090-5019
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Simvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA077691
Marketing category
ANDA
Substance
SIMVASTATIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-5019-090 TABLET, FILM COATED in 1 BOTTLE (50090-5019-0) 2020-04-24NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SimvastatinA-S Medication Solutions2025-04-25Human Prescription Drug Label5