enalapril maleate

Generic: enalapril maleate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-075
Product ID 71205-075_bdfcb7c8-7269-46a6-aff8-d73b093ee88a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA018998
Listing Expiration 2026-12-31
Marketing Start 1985-12-24

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 71205075
Hyphenated Format 71205-075

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 NDA018998 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-075-30)
  • 60 TABLET in 1 BOTTLE (71205-075-60)
  • 90 TABLET in 1 BOTTLE (71205-075-90)
source: ndc

Packages (3)

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": "bdfcb7c8-7269-46a6-aff8-d73b093ee88a", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["cc921315-8da1-487c-ba19-433470f5c8d8"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-075-30)", "package_ndc": "71205-075-30", "marketing_start_date": "20180702"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-075-60)", "package_ndc": "71205-075-60", "marketing_start_date": "20180702"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-075-90)", "package_ndc": "71205-075-90", "marketing_start_date": "20180702"}], "brand_name": "Enalapril Maleate", "product_id": "71205-075_bdfcb7c8-7269-46a6-aff8-d73b093ee88a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71205-075", "generic_name": "Enalapril Maleate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "NDA018998", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19851224", "listing_expiration_date": "20261231"}