Package 70518-4011-1

Brand: enalapril maleate

Generic: enalapril maleate
NDC Package

Package Facts

Identity

Package NDC 70518-4011-1
Digits Only 7051840111
Product NDC 70518-4011
Product ID 70518-4011_43df1c31-c8ac-2fa8-e063-6394a90abf79
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4011-1)

Marketing

Marketing Status
Marketed Since 2025-09-13
Brand enalapril maleate
Generic enalapril maleate
Sample Package No

Linked Drug Pages (1)

Enalapril Maleate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43df1c31-c8ac-2fa8-e063-6394a90abf79", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["e47afc0d-afc4-4972-a28a-5d3c640390ab"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4011-1)", "package_ndc": "70518-4011-1", "marketing_start_date": "20250913"}], "brand_name": "Enalapril Maleate", "product_id": "70518-4011_43df1c31-c8ac-2fa8-e063-6394a90abf79", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-4011", "generic_name": "Enalapril Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20240206", "listing_expiration_date": "20261231"}