simvastatin

Product NDC
50090-4897
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
simvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078155
Marketing category
ANDA
Substance
SIMVASTATIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-4897-090 TABLET, FILM COATED in 1 BOTTLE (50090-4897-0) 2020-02-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
simvastatinA-S Medication Solutions2023-02-04HUMAN PRESCRIPTION DRUG LABEL5