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Methylprednisolone - 59762-0049-1 - (METHYLPREDNISOLONE)

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Drug Information of Methylprednisolone

Product NDC: 59762-0049
Proprietary Name: Methylprednisolone
Non Proprietary Name: METHYLPREDNISOLONE
Active Ingredient(s): 8    mg/1 & nbsp;   METHYLPREDNISOLONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone

Product NDC: 59762-0049
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011153
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130403

Package Information of Methylprednisolone

Package NDC: 59762-0049-1
Package Description: 25 TABLET in 1 BOTTLE (59762-0049-1)

NDC Information of Methylprednisolone

NDC Code 59762-0049-1
Proprietary Name Methylprednisolone
Package Description 25 TABLET in 1 BOTTLE (59762-0049-1)
Product NDC 59762-0049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPREDNISOLONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130403
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Greenstone LLC
Substance Name METHYLPREDNISOLONE
Strength Number 8
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone


General Information