Package 50090-7670-0

Brand: ambrisentan

Generic: ambrisentan
NDC Package

Package Facts

Identity

Package NDC 50090-7670-0
Digits Only 5009076700
Product NDC 50090-7670
Description

30 TABLET, FILM COATED in 1 BOTTLE (50090-7670-0)

Marketing

Marketing Status
Marketed Since 2025-10-07
Brand ambrisentan
Generic ambrisentan
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a07dd73-2271-409b-a0b4-de0db982250e", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116"], "spl_set_id": ["a7dcdea4-d3da-4dc1-9193-6ebdb5b4e690"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7670-0)", "package_ndc": "50090-7670-0", "marketing_start_date": "20251007"}], "brand_name": "ambrisentan", "product_id": "50090-7670_0a07dd73-2271-409b-a0b4-de0db982250e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "50090-7670", "generic_name": "ambrisentan", "labeler_name": "A-S Medication Solutions", "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"}