enalapril maleate

Generic: enalapril maleate

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 20 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3820
Product ID 68071-3820_315b8a94-b7cd-1b47-e063-6294a90a2d39
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213273
Listing Expiration 2026-12-31
Marketing Start 2022-04-24

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 680713820
Hyphenated Format 68071-3820

Supplemental Identifiers

RxCUI
858810
UPC
0368071382037
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 ANDA213273 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (68071-3820-3)
source: ndc

Packages (1)

68071-3820-3 30 TABLET in 1 BOTTLE (68071-3820-3)

Ingredients (1)

enalapril maleate (20 mg/1)

Linked Drug Pages (1)

Enalapril Maleate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "315b8a94-b7cd-1b47-e063-6294a90a2d39", "openfda": {"upc": ["0368071382037"], "unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["315baaa6-512c-f27b-e063-6294a90a2c91"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3820-3)", "package_ndc": "68071-3820-3", "marketing_start_date": "20250327"}], "brand_name": "Enalapril Maleate", "product_id": "68071-3820_315b8a94-b7cd-1b47-e063-6294a90a2d39", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-3820", "generic_name": "Enalapril Maleate", "labeler_name": "NuCare Pharmaceuticals, 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": "20220424", "listing_expiration_date": "20261231"}