Package 70518-2023-1

Brand: solu-medrol

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 70518-2023-1
Digits Only 7051820231
Product NDC 70518-2023
Description

25 VIAL in 1 CARTON (70518-2023-1) / 2 mL in 1 VIAL (70518-2023-0)

Marketing

Marketing Status
Marketed Since 2019-04-15
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": "499b1561-882b-8553-e063-6294a90ad423", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704", "1743707"], "spl_set_id": ["1d5ef347-2e9a-432f-9a88-a7c4ba300267"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-2023-1)  / 2 mL in 1 VIAL (70518-2023-0)", "package_ndc": "70518-2023-1", "marketing_start_date": "20190415"}], "brand_name": "SOLU-MEDROL", "product_id": "70518-2023_499b1561-882b-8553-e063-6294a90ad423", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-2023", "generic_name": "methylprednisolone sodium succinate", "labeler_name": "REMEDYREPACK INC.", "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": "20190415", "listing_expiration_date": "20271231"}