Package 80425-0230-1
Brand: methylprednisolone
Generic: methylprednisolonePackage Facts
Identity
Package NDC
80425-0230-1
Digits Only
8042502301
Product NDC
80425-0230
Description
21 TABLET in 1 BLISTER PACK (80425-0230-1)
Marketing
Marketing Status
Brand
methylprednisolone
Generic
methylprednisolone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9b1617-60d1-f8ce-e063-6294a90ab02c", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["f19f3676-856f-e8d7-e053-2995a90ad703"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BLISTER PACK (80425-0230-1)", "package_ndc": "80425-0230-1", "marketing_start_date": "20230111"}], "brand_name": "Methylprednisolone", "product_id": "80425-0230_2a9b1617-60d1-f8ce-e063-6294a90ab02c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0230", "generic_name": "Methylprednisolone", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA040189", "marketing_category": "ANDA", "marketing_start_date": "20230111", "listing_expiration_date": "20261231"}