Medrol - 0009-0176-01 - (METHYLPREDNISOLONE)

Alphabetical Index


Drug Information of Medrol

Product NDC: 0009-0176
Proprietary Name: Medrol
Non Proprietary Name: METHYLPREDNISOLONE
Active Ingredient(s): 32    mg/1 & nbsp;   METHYLPREDNISOLONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Medrol

Product NDC: 0009-0176
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011153
Marketing Category: NDA
Start Marketing Date: 19571024

Package Information of Medrol

Package NDC: 0009-0176-01
Package Description: 25 TABLET in 1 BOTTLE (0009-0176-01)

NDC Information of Medrol

NDC Code 0009-0176-01
Proprietary Name Medrol
Package Description 25 TABLET in 1 BOTTLE (0009-0176-01)
Product NDC 0009-0176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPREDNISOLONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19571024
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name METHYLPREDNISOLONE
Strength Number 32
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Medrol


General Information