Package 80425-0482-1
Brand: prednisone
Generic: prednisonePackage Facts
Identity
Package NDC
80425-0482-1
Digits Only
8042504821
Product NDC
80425-0482
Description
21 TABLET in 1 BOTTLE, PLASTIC (80425-0482-1)
Marketing
Marketing Status
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": "31fa0646-b734-4e96-e063-6394a90a6b66", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["VB0R961HZT"], "rxcui": ["198145", "312615", "312617"], "spl_set_id": ["2d0562ad-6175-833c-e063-6394a90ad029"], "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, PLASTIC (80425-0482-1)", "package_ndc": "80425-0482-1", "marketing_start_date": "20250217"}], "brand_name": "prednisone", "product_id": "80425-0482_31fa0646-b734-4e96-e063-6394a90a6b66", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0482", "generic_name": "PREDNISONE", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prednisone", "active_ingredients": [{"name": "PREDNISONE", "strength": "5 mg/1"}], "application_number": "ANDA208412", "marketing_category": "ANDA", "marketing_start_date": "20250131", "listing_expiration_date": "20261231"}