enalapril maleate

Generic: enalapril maleate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1526
Product ID 63629-1526_fc88f6f7-f1a6-629f-e053-6294a90aa677
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075483
Listing Expiration 2026-12-31
Marketing Start 2009-12-11

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 636291526
Hyphenated Format 63629-1526

Supplemental Identifiers

RxCUI
858817
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
  • 10 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (63629-1526-1)
  • 30 TABLET in 1 BOTTLE (63629-1526-2)
  • 100 TABLET in 1 BOTTLE (63629-1526-3)
  • 90 TABLET in 1 BOTTLE (63629-1526-4)
  • 120 TABLET in 1 BOTTLE (63629-1526-5)
source: ndc

Packages (5)

Ingredients (1)

enalapril maleate (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc88f6f7-f1a6-629f-e053-6294a90aa677", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["5cc4f6f0-8925-81e1-b210-b5a4509a25a9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-1526-1)", "package_ndc": "63629-1526-1", "marketing_start_date": "20220208"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-1526-2)", "package_ndc": "63629-1526-2", "marketing_start_date": "20220208"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1526-3)", "package_ndc": "63629-1526-3", "marketing_start_date": "20220208"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-1526-4)", "package_ndc": "63629-1526-4", "marketing_start_date": "20101115"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-1526-5)", "package_ndc": "63629-1526-5", "marketing_start_date": "20220208"}], "brand_name": "ENALAPRIL MALEATE", "product_id": "63629-1526_fc88f6f7-f1a6-629f-e053-6294a90aa677", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "63629-1526", "generic_name": "ENALAPRIL MALEATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ENALAPRIL MALEATE", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA075483", "marketing_category": "ANDA", "marketing_start_date": "20091211", "listing_expiration_date": "20261231"}