Package 59651-494-30
Brand: ambrisentan
Generic: ambrisentanPackage Facts
Identity
Package NDC
59651-494-30
Digits Only
5965149430
Product NDC
59651-494
Description
30 TABLET, FILM COATED in 1 BOTTLE (59651-494-30)
Marketing
Marketing Status
Brand
ambrisentan
Generic
ambrisentan
Sample Package
No
Linked Drug Pages (1)
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 (59651-494-30)", "package_ndc": "59651-494-30", "marketing_start_date": "20220721"}], "brand_name": "ambrisentan", "product_id": "59651-494_a6d48e99-4411-4724-8372-b01692a5dff7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "59651-494", "generic_name": "ambrisentan", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ambrisentan", "active_ingredients": [{"name": "AMBRISENTAN", "strength": "5 mg/1"}], "application_number": "ANDA216531", "marketing_category": "ANDA", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}