SIMVASTATIN

Product NDC
60760-585
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SIMVASTATIN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
Application
ANDA078103
Marketing category
ANDA
Substance
SIMVASTATIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60760-585-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-585-30) 2023-04-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
SIMVASTATINST. MARY'S MEDICAL PARK PHARMACY2023-05-01HUMAN PRESCRIPTION DRUG LABEL1