Package 0009-0047-04

Brand: solu-medrol

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 0009-0047-04
Digits Only 0009004704
Product NDC 0009-0047
Description

25 VIAL in 1 CARTON (0009-0047-04) / 2 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1959-04-02
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": "f52c912a-f15e-457a-be68-56dd7f170d6d", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["207191", "207193", "311659", "314099", "1743704", "1743707"], "spl_set_id": ["7271310c-7764-4812-aa30-a5e90987c7a9"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0009-0047-04)  / 2 mL in 1 VIAL", "package_ndc": "0009-0047-04", "marketing_start_date": "19590402"}], "brand_name": "SOLU-MEDROL", "product_id": "0009-0047_f52c912a-f15e-457a-be68-56dd7f170d6d", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0009-0047", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "Pharmacia & Upjohn Company LLC", "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"}