ambrisentan

Generic: ambrisentan

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ambrisentan
Generic Name ambrisentan
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ambrisentan 10 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 59651-495
Product ID 59651-495_a6d48e99-4411-4724-8372-b01692a5dff7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216531
Listing Expiration 2026-12-31
Marketing Start 2022-07-21

Pharmacologic Class

Established (EPC)
endothelin receptor antagonist [epc]
Mechanism of Action
endothelin receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59651495
Hyphenated Format 59651-495

Supplemental Identifiers

RxCUI
722116 722122
UNII
HW6NV07QEC
NUI
N0000175581 N0000175364

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 ambrisentan (source: ndc)
Generic Name ambrisentan (source: ndc)
Application Number ANDA216531 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (59651-495-30)
source: ndc

Packages (1)

59651-495-30 30 TABLET, FILM COATED in 1 BOTTLE (59651-495-30)

Ingredients (1)

ambrisentan (10 mg/1)

Linked Drug Pages (1)

ambrisentan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a6d48e99-4411-4724-8372-b01692a5dff7", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116", "722122"], "spl_set_id": ["82e51c75-fb78-4ad3-8bce-5e0581d60014"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59651-495-30)", "package_ndc": "59651-495-30", "marketing_start_date": "20220721"}], "brand_name": "ambrisentan", "product_id": "59651-495_a6d48e99-4411-4724-8372-b01692a5dff7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "59651-495", "generic_name": "ambrisentan", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ambrisentan", "active_ingredients": [{"name": "AMBRISENTAN", "strength": "10 mg/1"}], "application_number": "ANDA216531", "marketing_category": "ANDA", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}