SIMVASTATIN

Product NDC
50090-6920
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SIMVASTATIN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078103
Marketing category
ANDA
Substance
SIMVASTATIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6920-090 TABLET, FILM COATED in 1 BOTTLE (50090-6920-0) 2023-12-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SIMVASTATINA-S Medication Solutions2026-03-23HUMAN PRESCRIPTION DRUG LABEL4