Dasatinib

Product NDC
70748-213
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dasatinib
Dosage form
TABLET
Route
ORAL
Labeler
Lupin Pharmaceuticals, Inc.
Application
ANDA214350
Marketing category
ANDA
Substance
DASATINIB
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70748-213-061 BOTTLE in 1 CARTON (70748-213-06) / 30 TABLET in 1 BOTTLE2026-01-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
DasatinibLupin Pharmaceuticals, Inc.2026-02-27HUMAN PRESCRIPTION DRUG LABEL7