Home > National Drug Code (NDC) > Depo-Medrol

Depo-Medrol - 0009-0280-51 - (methylprednisolone acetate)

Alphabetical Index


Drug Information of Depo-Medrol

Product NDC: 0009-0280
Proprietary Name: Depo-Medrol
Non Proprietary Name: methylprednisolone acetate
Active Ingredient(s): 40    mg/mL & nbsp;   methylprednisolone acetate
Administration Route(s): INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Depo-Medrol

Product NDC: 0009-0280
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: 0009-0280-51
Package Description: 25 VIAL, MULTI-DOSE in 1 PACKAGE (0009-0280-51) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Depo-Medrol

NDC Code 0009-0280-51
Proprietary Name Depo-Medrol
Package Description 25 VIAL, MULTI-DOSE in 1 PACKAGE (0009-0280-51) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0009-0280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylprednisolone acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Start Marketing Date 19590528
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Depo-Medrol


General Information