Cinacalcet

Product NDC
63629-8763
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Cinacalcet
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA210570
Marketing category
ANDA
Substance
CINACALCET HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-8763-130 TABLET, FILM COATED in 1 BOTTLE (63629-8763-1) 20190518NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
86fe67f9-d4e0-4966-a80b-c04bf6bb0ef9These highlights do not include all the information needed to use CINACALCET TABLETS safely and effectively. See full prescribing information for CINACALCET TABLETS. CINACALCET tablets , for oral use Initial U.S. Approval: 2004Bryant Ranch Prepack2023-10-30HUMAN PRESCRIPTION DRUG LABEL105