Enalapril maleate

Product NDC
23155-773
11-digit product format
231550773
Labeler code
23155
Product ID
23155-773_f59f9ce5-246c-47c9-a171-aee4cc1c09a3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Enalapril maleate
Dosage form
TABLET
Route
ORAL
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Application
ANDA075479
Marketing category
ANDA
Marketing start
2020-10-01
Substance
ENALAPRIL MALEATE
Active strength
20 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
23155-773-0123155077301100 TABLET in 1 BOTTLE (23155-773-01) 100 tablet2020-10-01NoNoHistorical
23155-773-0523155077305500 TABLET in 1 BOTTLE (23155-773-05) 500 tablet2020-10-01NoNoHistorical
23155-773-10231550773101000 TABLET in 1 BOTTLE (23155-773-10) 1000 tablet2020-10-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rx onlyLegacy Pharmaceutical Packaging, LLC2026-03-11HUMAN PRESCRIPTION DRUG LABEL8
Rx onlyMajor Pharmaceuticals2026-01-30HUMAN PRESCRIPTION DRUG LABEL3
Rx onlyNorthwind Health Company, LLC2026-01-01HUMAN PRESCRIPTION DRUG LABEL4
Rx onlyHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.2025-12-30HUMAN PRESCRIPTION DRUG LABEL7
Rx onlyREMEDYREPACK INC.2025-09-26HUMAN PRESCRIPTION DRUG LABEL3
Rx onlyA-S Medication Solutions2023-04-27HUMAN PRESCRIPTION DRUG LABEL3