enalapril maleate

Generic: enalapril maleate

Labeler: directrx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler directrx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 2.5 mg/1

Manufacturer
DirectRx

Identifiers & Regulatory

Product NDC 72189-282
Product ID 72189-282_2c29035b-2eb7-2267-e063-6394a90a93d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075483
Listing Expiration 2026-12-31
Marketing Start 2021-10-19

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] decreased blood pressure [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189282
Hyphenated Format 72189-282

Supplemental Identifiers

RxCUI
858804
UNII
9O25354EPJ

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name enalapril maleate (source: ndc)
Generic Name enalapril maleate (source: ndc)
Application Number ANDA075483 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72189-282-30)
  • 90 TABLET in 1 BOTTLE (72189-282-90)
source: ndc

Packages (2)

Ingredients (1)

enalapril maleate (2.5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c29035b-2eb7-2267-e063-6394a90a93d4", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858804"], "spl_set_id": ["ceb49e77-a821-35b8-e053-2a95a90a7e53"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-282-30)", "package_ndc": "72189-282-30", "marketing_start_date": "20211019"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-282-90)", "package_ndc": "72189-282-90", "marketing_start_date": "20211019"}], "brand_name": "ENALAPRIL MALEATE", "product_id": "72189-282_2c29035b-2eb7-2267-e063-6394a90a93d4", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72189-282", "generic_name": "ENALAPRIL MALEATE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENALAPRIL MALEATE", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "2.5 mg/1"}], "application_number": "ANDA075483", "marketing_category": "ANDA", "marketing_start_date": "20211019", "listing_expiration_date": "20261231"}