Package 84549-039-28

Brand: solu-medrol

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 84549-039-28
Digits Only 8454903928
Product NDC 84549-039
Description

1 mL in 1 VIAL (84549-039-28)

Marketing

Marketing Status
Marketed Since 2025-10-10
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": "463eae7b-ee0e-b775-e063-6394a90ae2c3", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["207191", "311659"], "spl_set_id": ["42df21df-9284-4505-e063-6294a90a7024"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (84549-039-28)", "package_ndc": "84549-039-28", "marketing_start_date": "20251010"}], "brand_name": "SOLU-MEDROL", "product_id": "84549-039_463eae7b-ee0e-b775-e063-6394a90ae2c3", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "84549-039", "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": "40 mg/mL"}], "application_number": "NDA011856", "marketing_category": "NDA", "marketing_start_date": "19590402", "listing_expiration_date": "20261231"}