Package 84549-047-22

Brand: solu-medrol

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 84549-047-22
Digits Only 8454904722
Product NDC 84549-047
Description

2 mL in 1 VIAL (84549-047-22)

Marketing

Marketing Status
Marketed Since 2025-08-27
Brand solu-medrol
Generic methylprednisolone sodium succinate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3a38d1c4-e75d-f6e9-e063-6394a90a888b", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704", "1743707"], "spl_set_id": ["38698075-ac58-b5a4-e063-6294a90a7848"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "2 mL in 1 VIAL (84549-047-22)", "package_ndc": "84549-047-22", "marketing_start_date": "20250827"}], "brand_name": "SOLU-MEDROL", "product_id": "84549-047_3a38d1c4-e75d-f6e9-e063-6394a90a888b", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "84549-047", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLU-MEDROL", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "125 mg/2mL"}], "application_number": "NDA011856", "marketing_category": "NDA", "marketing_start_date": "19590402", "listing_expiration_date": "20261231"}