Package 80425-0485-1

Brand: prednisone

Generic: prednisone
NDC Package

Package Facts

Identity

Package NDC 80425-0485-1
Digits Only 8042504851
Product NDC 80425-0485
Description

21 TABLET in 1 BOTTLE (80425-0485-1)

Marketing

Marketing Status
Marketed Since 2025-02-14
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": "2e630ab1-d110-28f4-e063-6394a90af942", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312617"], "spl_set_id": ["2e630aa1-eccd-f5eb-e063-6294a90a4745"], "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": "21 TABLET in 1 BOTTLE (80425-0485-1)", "package_ndc": "80425-0485-1", "marketing_start_date": "20250214"}], "brand_name": "PredniSONE", "product_id": "80425-0485_2e630ab1-d110-28f4-e063-6394a90af942", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0485", "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": "ANDA084122", "marketing_category": "ANDA", "marketing_start_date": "20250214", "listing_expiration_date": "20261231"}