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 5 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7222
Product ID 50090-7222_012e4c94-e23e-49b8-9241-29c3567c441d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075479
Listing Expiration 2026-12-31
Marketing Start 2020-04-28

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 500907222
Hyphenated Format 50090-7222

Supplemental Identifiers

RxCUI
858813
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 ANDA075479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (50090-7222-0)
  • 100 TABLET in 1 BOTTLE (50090-7222-1)
  • 90 TABLET in 1 BOTTLE (50090-7222-3)
source: ndc

Packages (3)

Ingredients (1)

enalapril maleate (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "012e4c94-e23e-49b8-9241-29c3567c441d", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858813"], "spl_set_id": ["9f913e79-fe6d-4ff2-9f8e-eef9df689fa8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7222-0)", "package_ndc": "50090-7222-0", "marketing_start_date": "20240813"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7222-1)", "package_ndc": "50090-7222-1", "marketing_start_date": "20240813"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7222-3)", "package_ndc": "50090-7222-3", "marketing_start_date": "20240813"}], "brand_name": "Enalapril maleate", "product_id": "50090-7222_012e4c94-e23e-49b8-9241-29c3567c441d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50090-7222", "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": "5 mg/1"}], "application_number": "ANDA075479", "marketing_category": "ANDA", "marketing_start_date": "20200428", "listing_expiration_date": "20261231"}