enalapril maleate
Generic: enalapril maleate
Labeler: oceanside pharmaceuticalsDrug Facts
Product Profile
Brand Name
enalapril maleate
Generic Name
enalapril maleate
Labeler
oceanside pharmaceuticals
Dosage Form
TABLET
Routes
Active Ingredients
enalapril maleate 2.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68682-710
Product ID
68682-710_6771388d-89b3-43ec-b69e-9cebeaa2a00a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA018998
Listing Expiration
2026-12-31
Marketing Start
1988-07-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68682710
Hyphenated Format
68682-710
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 2.5 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (68682-710-01)
- 1000 TABLET in 1 BOTTLE (68682-710-10)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6771388d-89b3-43ec-b69e-9cebeaa2a00a", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858804", "858810", "858813", "858817"], "spl_set_id": ["ebd2a62d-a704-4f8a-a104-749a5296502f"], "manufacturer_name": ["OCEANSIDE PHARMACEUTICALS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68682-710-01)", "package_ndc": "68682-710-01", "marketing_start_date": "19880726"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68682-710-10)", "package_ndc": "68682-710-10", "marketing_start_date": "19880726"}], "brand_name": "Enalapril Maleate", "product_id": "68682-710_6771388d-89b3-43ec-b69e-9cebeaa2a00a", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68682-710", "generic_name": "Enalapril Maleate", "labeler_name": "OCEANSIDE PHARMACEUTICALS", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "2.5 mg/1"}], "application_number": "NDA018998", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19880726", "listing_expiration_date": "20261231"}