enalapril maleate
Generic: enalapril maleate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
enalapril maleate
Generic Name
enalapril maleate
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
enalapril maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4256
Product ID
70518-4256_4008b194-eaf3-53aa-e063-6394a90ac6ce
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075657
Listing Expiration
2026-12-31
Marketing Start
2025-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184256
Hyphenated Format
70518-4256
Supplemental Identifiers
RxCUI
UNII
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
ANDA075657 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BLISTER PACK (70518-4256-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4008b194-eaf3-53aa-e063-6394a90ac6ce", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["3fbc6cce-7ad5-49d5-9705-5f66ef92d544"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4256-0)", "package_ndc": "70518-4256-0", "marketing_start_date": "20250115"}], "brand_name": "Enalapril Maleate", "product_id": "70518-4256_4008b194-eaf3-53aa-e063-6394a90ac6ce", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "70518-4256", "generic_name": "Enalapril Maleate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA075657", "marketing_category": "ANDA", "marketing_start_date": "20250115", "listing_expiration_date": "20261231"}