enalapril maleate

Generic: enalapril maleate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 5 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-705
Product ID 23155-705_f59f9ce5-246c-47c9-a171-aee4cc1c09a3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075479
Listing Expiration 2026-12-31
Marketing Start 2020-04-28

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 23155705
Hyphenated Format 23155-705

Supplemental Identifiers

RxCUI
858804 858810 858813 858817
UPC
0323155706017 0323155773019 0323155705010 0323155772012 0323155704013 0323155707014
UNII
9O25354EPJ

Packaging Origin

Original Packager
true

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 ANDA075479 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-705-01)
  • 1000 TABLET in 1 BOTTLE (23155-705-10)
source: ndc

Packages (2)

23155-705-01 100 TABLET in 1 BOTTLE (23155-705-01) 23155-705-10 1000 TABLET in 1 BOTTLE (23155-705-10)

Ingredients (1)

enalapril maleate (5 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": "f59f9ce5-246c-47c9-a171-aee4cc1c09a3", "openfda": {"upc": ["0323155706017", "0323155773019", "0323155705010", "0323155772012", "0323155704013", "0323155707014"], "unii": ["9O25354EPJ"], "rxcui": ["858804", "858810", "858813", "858817"], "spl_set_id": ["5c49fb37-1f09-4965-b213-5580d3a30a11"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-705-01)", "package_ndc": "23155-705-01", "marketing_start_date": "20200428"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-705-10)", "package_ndc": "23155-705-10", "marketing_start_date": "20200428"}], "brand_name": "Enalapril maleate", "product_id": "23155-705_f59f9ce5-246c-47c9-a171-aee4cc1c09a3", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "23155-705", "generic_name": "Enalapril maleate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "5 mg/1"}], "application_number": "ANDA075479", "marketing_category": "ANDA", "marketing_start_date": "20200428", "listing_expiration_date": "20261231"}