Anastrozole

Product NDC
68071-1543
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Anastrozole
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA090568
Marketing category
ANDA
Substance
ANASTROZOLE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-1543-990 TABLET in 1 BOTTLE, PLASTIC (68071-1543-9) 2022-12-09NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AnastrozoleNuCare Pharmaceuticals,Inc.2024-04-05HUMAN PRESCRIPTION DRUG LABEL2