enalapril maleate

Generic: enalapril maleate

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name enalapril maleate
Generic Name enalapril maleate
Labeler northwind health company, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

enalapril maleate 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-341
Product ID 51655-341_48eb2d46-5438-a385-e063-6294a90a0fc7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075657
Listing Expiration 2027-12-31
Marketing Start 2020-05-28

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 51655341
Hyphenated Format 51655-341

Supplemental Identifiers

RxCUI
858810
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 ANDA075657 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE, PLASTIC (51655-341-26)
source: ndc

Packages (1)

51655-341-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-341-26)

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": "48eb2d46-5438-a385-e063-6294a90a0fc7", "openfda": {"unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["ab2ffb6e-4628-e44c-e053-2a95a90a2336"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-341-26)", "package_ndc": "51655-341-26", "marketing_start_date": "20200528"}], "brand_name": "Enalapril Maleate", "product_id": "51655-341_48eb2d46-5438-a385-e063-6294a90a0fc7", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51655-341", "generic_name": "Enalapril Maleate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Enalapril Maleate", "active_ingredients": [{"name": "ENALAPRIL MALEATE", "strength": "20 mg/1"}], "application_number": "ANDA075657", "marketing_category": "ANDA", "marketing_start_date": "20200528", "listing_expiration_date": "20271231"}