Package 80425-0491-1

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 80425-0491-1
Digits Only 8042504911
Product NDC 80425-0491
Description

1 BLISTER PACK in 1 CARTON (80425-0491-1) / 21 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-03-17
Brand prednisone
Generic prednisone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "309580ae-7ca3-e291-e063-6394a90adbc7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145"], "spl_set_id": ["309580a7-c3bb-e53b-e063-6394a90a1563"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (80425-0491-1)  / 21 TABLET in 1 BLISTER PACK", "package_ndc": "80425-0491-1", "marketing_start_date": "20250317"}], "brand_name": "Prednisone", "product_id": "80425-0491_309580ae-7ca3-e291-e063-6394a90adbc7", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0491", "generic_name": "Prednisone", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "10 mg/1"}], "application_number": "ANDA085162", "marketing_category": "ANDA", "marketing_start_date": "20250317", "listing_expiration_date": "20261231"}