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Methylprednisolone - 63629-3910-1 - (Methylprednisolone)

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Drug Information of Methylprednisolone

Product NDC: 63629-3910
Proprietary Name: Methylprednisolone
Non Proprietary Name: Methylprednisolone
Active Ingredient(s): 4    mg/1 & nbsp;   Methylprednisolone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone

Product NDC: 63629-3910
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040189
Marketing Category: ANDA
Start Marketing Date: 19971031

Package Information of Methylprednisolone

Package NDC: 63629-3910-1
Package Description: 30 TABLET in 1 BOTTLE (63629-3910-1)

NDC Information of Methylprednisolone

NDC Code 63629-3910-1
Proprietary Name Methylprednisolone
Package Description 30 TABLET in 1 BOTTLE (63629-3910-1)
Product NDC 63629-3910
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylprednisolone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19971031
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name METHYLPREDNISOLONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone


General Information