enalapril maleate

Generic: enalapril maleate

Labeler: preferred pharmaceuicals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler preferred pharmaceuicals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 10 mg/1

Manufacturer
Preferred Pharmaceuicals Inc.

Identifiers & Regulatory

Product NDC 68788-8385
Product ID 68788-8385_4cfa9a66-5f35-4b5b-adda-9546156f7bb0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213273
Listing Expiration 2026-12-31
Marketing Start 2023-03-01

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 687888385
Hyphenated Format 68788-8385

Supplemental Identifiers

RxCUI
858817
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
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-8385-1)
  • 30 TABLET in 1 BOTTLE (68788-8385-3)
  • 60 TABLET in 1 BOTTLE (68788-8385-6)
  • 90 TABLET in 1 BOTTLE (68788-8385-9)
source: ndc

Packages (4)

68788-8385-1 100 TABLET in 1 BOTTLE (68788-8385-1) 68788-8385-3 30 TABLET in 1 BOTTLE (68788-8385-3) 68788-8385-6 60 TABLET in 1 BOTTLE (68788-8385-6) 68788-8385-9 90 TABLET in 1 BOTTLE (68788-8385-9)

Ingredients (1)

enalapril maleate (10 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": "4cfa9a66-5f35-4b5b-adda-9546156f7bb0", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858817"], "spl_set_id": ["898b36d6-320f-4d6c-9734-0be8363dc3d7"], "manufacturer_name": ["Preferred Pharmaceuicals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8385-1)", "package_ndc": "68788-8385-1", "marketing_start_date": "20230301"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8385-3)", "package_ndc": "68788-8385-3", "marketing_start_date": "20230301"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8385-6)", "package_ndc": "68788-8385-6", "marketing_start_date": "20230301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8385-9)", "package_ndc": "68788-8385-9", "marketing_start_date": "20230301"}], "brand_name": "Enalapril Maleate", "product_id": "68788-8385_4cfa9a66-5f35-4b5b-adda-9546156f7bb0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-8385", "generic_name": "Enalapril Maleate", "labeler_name": "Preferred Pharmaceuicals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "10 mg/1"}], "application_number": "ANDA213273", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}