Package 72578-166-01

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 72578-166-01
Digits Only 7257816601
Product NDC 72578-166
Description

100 TABLET in 1 BOTTLE (72578-166-01)

Marketing

Marketing Status
Marketed Since 2024-05-13
Brand dexamethasone
Generic dexamethasone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "57d9469e-8d0d-4a58-a56c-3c266fe36b74", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197579"], "spl_set_id": ["360d3af0-8f69-4e82-ab5f-1f70cc2025d4"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72578-166-01)", "package_ndc": "72578-166-01", "marketing_start_date": "20240513"}], "brand_name": "Dexamethasone", "product_id": "72578-166_57d9469e-8d0d-4a58-a56c-3c266fe36b74", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72578-166", "generic_name": "Dexamethasone", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "1 mg/1"}], "application_number": "ANDA216284", "marketing_category": "ANDA", "marketing_start_date": "20240513", "listing_expiration_date": "20261231"}