Enalapril Maleate

Product NDC
68071-3537
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Enalapril Maleate
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA213273
Marketing category
ANDA
Substance
ENALAPRIL MALEATE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68071-3537-330 TABLET in 1 BOTTLE (68071-3537-3) 2023-11-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ENALAPRIL MALEATE TABLETS Rx onlyNuCare Pharmaceuticals,Inc.2025-02-03HUMAN PRESCRIPTION DRUG LABEL2