enalapril maleate

Generic: enalapril maleate

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 20 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7677
Product ID 50090-7677_68698c51-6c2c-425e-a681-fbb382d79968
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075178
Listing Expiration 2026-12-31
Marketing Start 2025-02-12

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 500907677
Hyphenated Format 50090-7677

Supplemental Identifiers

RxCUI
858810
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 ANDA075178 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7677-0)
  • 60 TABLET in 1 BOTTLE (50090-7677-1)
  • 90 TABLET in 1 BOTTLE (50090-7677-3)
source: ndc

Packages (3)

50090-7677-0 30 TABLET in 1 BOTTLE (50090-7677-0) 50090-7677-1 60 TABLET in 1 BOTTLE (50090-7677-1) 50090-7677-3 90 TABLET in 1 BOTTLE (50090-7677-3)

Ingredients (1)

enalapril maleate (20 mg/1)

Linked Drug Pages (1)

ENALAPRIL MALEATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "68698c51-6c2c-425e-a681-fbb382d79968", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["fd0a7ecc-d6a2-4e04-a14f-1ed4dacb7df3"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7677-0)", "package_ndc": "50090-7677-0", "marketing_start_date": "20251008"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7677-1)", "package_ndc": "50090-7677-1", "marketing_start_date": "20251008"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7677-3)", "package_ndc": "50090-7677-3", "marketing_start_date": "20251008"}], "brand_name": "ENALAPRIL MALEATE", "product_id": "50090-7677_68698c51-6c2c-425e-a681-fbb382d79968", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-7677", "generic_name": "ENALAPRIL MALEATE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENALAPRIL MALEATE", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075178", "marketing_category": "ANDA", "marketing_start_date": "20250212", "listing_expiration_date": "20261231"}