Package 47335-237-85

{"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"}