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Depo-Medrol - 0009-3475-03 - (METHYLPREDNISOLONE ACETATE)

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Drug Information of Depo-Medrol

Product NDC: 0009-3475
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: 0009-3475
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011757
Marketing Category: NDA
Start Marketing Date: 19590528

Package Information of Depo-Medrol

Package NDC: 0009-3475-03
Package Description: 25 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3475-03) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Depo-Medrol

NDC Code 0009-3475-03
Proprietary Name Depo-Medrol
Package Description 25 VIAL, SINGLE-DOSE in 1 PACKAGE (0009-3475-03) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0009-3475
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 Pharmacia and Upjohn Company
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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