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SOLU-MEDROL - 55154-3915-5 - (methylprednisolone sodium succinate)

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Drug Information of SOLU-MEDROL

Product NDC: 55154-3915
Proprietary Name: SOLU-MEDROL
Non Proprietary Name: methylprednisolone sodium succinate
Active Ingredient(s): 125    mg/mL & nbsp;   methylprednisolone sodium succinate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SOLU-MEDROL

Product NDC: 55154-3915
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011856
Marketing Category: NDA
Start Marketing Date: 19590402

Package Information of SOLU-MEDROL

Package NDC: 55154-3915-5
Package Description: 5 VIAL, PATENT DELIVERY SYSTEM in 1 BAG (55154-3915-5) > 2 mL in 1 VIAL, PATENT DELIVERY SYSTEM

NDC Information of SOLU-MEDROL

NDC Code 55154-3915-5
Proprietary Name SOLU-MEDROL
Package Description 5 VIAL, PATENT DELIVERY SYSTEM in 1 BAG (55154-3915-5) > 2 mL in 1 VIAL, PATENT DELIVERY SYSTEM
Product NDC 55154-3915
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylprednisolone sodium succinate
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19590402
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
Strength Number 125
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of SOLU-MEDROL


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