Enalapril Maleate

Product NDC
71335-2382
11-digit product format
713352382
Labeler code
71335
Product ID
71335-2382_dbc135b7-2702-4b80-b25b-7fa512021345
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Enalapril Maleate
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213273
Marketing category
ANDA
Marketing start
2022-04-24
Substance
ENALAPRIL MALEATE
Active strength
5 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
9O25354EPJENALAPRIL MALEATE76095-16-4ENALAPRIL MALEATE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2382-171335238201150 TABLET in 1 BOTTLE (71335-2382-1) 150 tablet2024-07-08NoNoHistorical
71335-2382-271335238202100 TABLET in 1 BOTTLE (71335-2382-2) 100 tablet2024-07-08NoNoHistorical
71335-2382-37133523820330 TABLET in 1 BOTTLE (71335-2382-3) 30 tablet2024-07-08NoNoHistorical
71335-2382-47133523820460 TABLET in 1 BOTTLE (71335-2382-4) 60 tablet2024-07-08NoNoHistorical
71335-2382-57133523820590 TABLET in 1 BOTTLE (71335-2382-5) 90 tablet2024-07-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ENALAPRIL MALEATE TABLETS Rx onlyBryant Ranch Prepack2025-03-31HUMAN PRESCRIPTION DRUG LABEL2