Package 82009-141-30

Brand: ambrisentan

Generic: ambrisentan
NDC Package

Package Facts

Identity

Package NDC 82009-141-30
Digits Only 8200914130
Product NDC 82009-141
Description

30 TABLET, FILM COATED in 1 BOTTLE (82009-141-30)

Marketing

Marketing Status
Marketed Since 2024-05-01
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": "64a9be1d-a83b-40aa-942f-18c6a9382dfa", "openfda": {"nui": ["N0000175581", "N0000175364"], "unii": ["HW6NV07QEC"], "rxcui": ["722116", "722122"], "spl_set_id": ["6fc6032f-94dc-4067-8b24-01990ec99db0"], "pharm_class_epc": ["Endothelin Receptor Antagonist [EPC]"], "pharm_class_moa": ["Endothelin Receptor Antagonists [MoA]"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82009-141-30)", "package_ndc": "82009-141-30", "marketing_start_date": "20240501"}], "brand_name": "Ambrisentan", "product_id": "82009-141_64a9be1d-a83b-40aa-942f-18c6a9382dfa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Endothelin Receptor Antagonist [EPC]", "Endothelin Receptor Antagonists [MoA]"], "product_ndc": "82009-141", "generic_name": "Ambrisentan", "labeler_name": "Quallent Pharmaceuticals Health LLC", "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": "20240501", "listing_expiration_date": "20271231"}