Package 70710-1179-8

Brand: ambrisentan

Generic: ambrisentan
NDC Package

Package Facts

Identity

Package NDC 70710-1179-8
Digits Only 7071011798
Product NDC 70710-1179
Description

3 BLISTER PACK in 1 CARTON (70710-1179-8) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-04-12
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": "4ad0e26d-a3b2-47d1-89a0-6e7e0697d5e4", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116", "722122"], "spl_set_id": ["37af3191-0ed3-4783-8747-065f1462f2d2"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1179-1)", "package_ndc": "70710-1179-1", "marketing_start_date": "20190412"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70710-1179-3)", "package_ndc": "70710-1179-3", "marketing_start_date": "20190412"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (70710-1179-7)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70710-1179-7", "marketing_start_date": "20190412"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70710-1179-8)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70710-1179-8", "marketing_start_date": "20190412"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70710-1179-9)", "package_ndc": "70710-1179-9", "marketing_start_date": "20190412"}], "brand_name": "Ambrisentan", "product_id": "70710-1179_4ad0e26d-a3b2-47d1-89a0-6e7e0697d5e4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "70710-1179", "generic_name": "Ambrisentan", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ambrisentan", "active_ingredients": [{"name": "AMBRISENTAN", "strength": "5 mg/1"}], "application_number": "ANDA210058", "marketing_category": "ANDA", "marketing_start_date": "20190412", "listing_expiration_date": "20261231"}