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Depo-Medrol - 54868-1185-1 - (methylprednisolone acetate)

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Drug Information of Depo-Medrol

Product NDC: 54868-1185
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: 54868-1185
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011757
Marketing Category: NDA
Start Marketing Date: 20070206

Package Information of Depo-Medrol

Package NDC: 54868-1185-1
Package Description: 25 VIAL, SINGLE-DOSE in 1 PACKAGE (54868-1185-1) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Depo-Medrol

NDC Code 54868-1185-1
Proprietary Name Depo-Medrol
Package Description 25 VIAL, SINGLE-DOSE in 1 PACKAGE (54868-1185-1) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 54868-1185
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 20070206
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
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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