ambrisentan

Generic: ambrisentan

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ambrisentan
Generic Name ambrisentan
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ambrisentan 10 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-237
Product ID 47335-237_294580cb-5622-4f48-89a8-99000a7a2964
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210784
Listing Expiration 2026-12-31
Marketing Start 2019-04-29

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 47335237
Hyphenated Format 47335-237

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 ANDA210784 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (47335-237-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
  • 1 BLISTER PACK in 1 CARTON (47335-237-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
  • 30 TABLET, FILM COATED in 1 BOTTLE (47335-237-83)
  • 10 TABLET, FILM COATED in 1 BOTTLE (47335-237-85)
source: ndc

Packages (4)

Ingredients (1)

ambrisentan (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "294580cb-5622-4f48-89a8-99000a7a2964", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116", "722122"], "spl_set_id": ["a4978a54-1799-43d6-85dd-05fa9de0a5d7"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (47335-237-64)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)", "package_ndc": "47335-237-64", "marketing_start_date": "20190429"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (47335-237-66)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)", "package_ndc": "47335-237-66", "marketing_start_date": "20190429"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-237-83)", "package_ndc": "47335-237-83", "marketing_start_date": "20190429"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (47335-237-85)", "package_ndc": "47335-237-85", "marketing_start_date": "20190429"}], "brand_name": "ambrisentan", "product_id": "47335-237_294580cb-5622-4f48-89a8-99000a7a2964", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "47335-237", "generic_name": "ambrisentan", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ambrisentan", "active_ingredients": [{"name": "AMBRISENTAN", "strength": "10 mg/1"}], "application_number": "ANDA210784", "marketing_category": "ANDA", "marketing_start_date": "20190429", "listing_expiration_date": "20261231"}