Atorvastatin Calcium

Product NDC
68071-3891
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
atorvastatin calcium, film coated
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA209912
Marketing category
ANDA
Substance
ATORVASTATIN CALCIUM TRIHYDRATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3891-330 TABLET in 1 BOTTLE (68071-3891-3) 2025-09-16NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Atorvastatin CalciumNuCare Pharmaceuticals, Inc.2025-09-16HUMAN PRESCRIPTION DRUG LABEL1