Sacubitril and Valsartan

Product NDC
60687-955
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sacubitril and Valsartan
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
American Health Packaging
Application
ANDA213611
Marketing category
ANDA
Substance
SACUBITRIL; VALSARTAN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
60687-955-5760 BLISTER PACK in 1 CARTON (60687-955-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-955-11) 2026-05-01NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Sacubitril and ValsartanAmerican Health Packaging2026-05-15HUMAN PRESCRIPTION DRUG LABEL1