enalapril maleate

Generic: enalapril maleate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

enalapril maleate 20 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-318
Product ID 72789-318_2e70221c-7705-77b8-e063-6394a90a32a6
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 72789318
Hyphenated Format 72789-318

Supplemental Identifiers

RxCUI
858810
UPC
0372789318905
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
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-318-90)
source: ndc

Packages (1)

72789-318-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-318-90)

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": "2e70221c-7705-77b8-e063-6394a90a32a6", "openfda": {"upc": ["0372789318905"], "unii": ["9O25354EPJ"], "rxcui": ["858810"], "spl_set_id": ["cbaaa849-0f9d-4294-b122-090ff17fdcc7"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-318-90)", "package_ndc": "72789-318-90", "marketing_start_date": "20230404"}], "brand_name": "Enalapril Maleate", "product_id": "72789-318_2e70221c-7705-77b8-e063-6394a90a32a6", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "72789-318", "generic_name": "Enalapril Maleate", "labeler_name": "PD-Rx 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"}