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Depo-Medrol - 55154-3932-5 - (methylprednisolone acetate)

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Drug Information of Depo-Medrol

Product NDC: 55154-3932
Proprietary Name: Depo-Medrol
Non Proprietary Name: methylprednisolone acetate
Active Ingredient(s): 80    mg/mL & nbsp;   methylprednisolone acetate
Administration Route(s): INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Depo-Medrol

Product NDC: 55154-3932
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011757
Marketing Category: NDA
Start Marketing Date: 19590528

Package Information of Depo-Medrol

Package NDC: 55154-3932-5
Package Description: 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3932-5) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Depo-Medrol

NDC Code 55154-3932-5
Proprietary Name Depo-Medrol
Package Description 5 VIAL, SINGLE-DOSE in 1 BAG (55154-3932-5) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55154-3932
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylprednisolone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
Start Marketing Date 19590528
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 80
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Depo-Medrol


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