ATORVASTATIN CALCIUM

Product NDC
68071-3628
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ATORVASTATIN CALCIUM
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc,
Application
ANDA214344
Marketing category
ANDA
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3628-990 TABLET, FILM COATED in 1 BOTTLE (68071-3628-9) 2024-06-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ATORVASTATIN CALCIUMNuCare Pharmaceuticals,Inc, | NuCare Pharmaceuticals,Inc.2024-06-14HUMAN PRESCRIPTION DRUG LABEL1