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Depo-Medrol - 49349-948-01 - (methylprednisolone acetate)

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Drug Information of Depo-Medrol

Product NDC: 49349-948
Proprietary Name: Depo-Medrol
Non Proprietary Name: methylprednisolone acetate
Active Ingredient(s): 40    mg/1 & nbsp;   methylprednisolone acetate
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Depo-Medrol

Product NDC: 49349-948
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011757
Marketing Category: NDA
Start Marketing Date: 20130410

Package Information of Depo-Medrol

Package NDC: 49349-948-01
Package Description: 1 INJECTION, SUSPENSION in 1 CARTON (49349-948-01)

NDC Information of Depo-Medrol

NDC Code 49349-948-01
Proprietary Name Depo-Medrol
Package Description 1 INJECTION, SUSPENSION in 1 CARTON (49349-948-01)
Product NDC 49349-948
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylprednisolone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR
Start Marketing Date 20130410
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Depo-Medrol


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