Package 72189-264-21
Brand: methylprednisolone
Generic: methylprednisolonePackage Facts
Identity
Package NDC
72189-264-21
Digits Only
7218926421
Product NDC
72189-264
Description
21 TABLET in 1 BOTTLE (72189-264-21)
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": "2c28f93c-99a2-f643-e063-6394a90a6f9d", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["8c3f3f63-8a05-7a4a-e053-2995a90ad95a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-264-21)", "package_ndc": "72189-264-21", "marketing_start_date": "20210913"}], "brand_name": "METHYLPREDNISOLONE", "product_id": "72189-264_2c28f93c-99a2-f643-e063-6394a90a6f9d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-264", "generic_name": "METHYLPREDNISOLONE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPREDNISOLONE", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA204072", "marketing_category": "ANDA", "marketing_start_date": "20210913", "listing_expiration_date": "20261231"}