Package 0009-0047-22

Brand: solu-medrol

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 0009-0047-22
Digits Only 0009004722
Product NDC 0009-0047
Description

25 VIAL in 1 CARTON (0009-0047-22) / 2 mL in 1 VIAL (0009-0047-25)

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": "c157d266-8633-4c2e-ae1f-0207e4f19b35", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["207191", "207193", "311659", "314099", "1357886", "1357888", "1743704", "1743707", "1743720", "1743722", "1743726", "1743729"], "spl_set_id": ["cd99be87-c8d9-48d6-a8e5-e081052e3f19"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (0009-0047-22)  / 2 mL in 1 VIAL (0009-0047-25)", "package_ndc": "0009-0047-22", "marketing_start_date": "19590402"}, {"sample": false, "description": "25 VIAL in 1 CARTON (0009-0047-26)  / 2 mL in 1 VIAL (0009-0047-27)", "package_ndc": "0009-0047-26", "marketing_start_date": "19590402"}], "brand_name": "SOLU-MEDROL", "product_id": "0009-0047_c157d266-8633-4c2e-ae1f-0207e4f19b35", "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"}