enalapril maleate
Generic: enalapril maleate
Labeler: legacy pharmaceutical packaging, llcDrug Facts
Product Profile
Brand Name
enalapril maleate
Generic Name
enalapril maleate
Labeler
legacy pharmaceutical packaging, llc
Dosage Form
TABLET
Routes
Active Ingredients
enalapril maleate 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68645-456
Product ID
68645-456_30129941-9087-89ee-e063-6394a90aaba1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075483
Listing Expiration
2026-12-31
Marketing Start
2009-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68645456
Hyphenated Format
68645-456
Supplemental Identifiers
RxCUI
UPC
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
ANDA075483 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (68645-456-90)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30129941-9087-89ee-e063-6394a90aaba1", "openfda": {"upc": ["0368645457901", "0368645456904", "0368645455907"], "unii": ["9O25354EPJ"], "rxcui": ["858810", "858813", "858817"], "spl_set_id": ["b156108d-2381-47ce-8e5e-14d723d03b88"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68645-456-90)", "package_ndc": "68645-456-90", "marketing_start_date": "20091211"}], "brand_name": "ENALAPRIL MALEATE", "product_id": "68645-456_30129941-9087-89ee-e063-6394a90aaba1", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68645-456", "generic_name": "ENALAPRIL MALEATE", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "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"}