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Methylprednisolone - 49349-750-05 - (METHYLPREDNISOLONE)

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Drug Information of Methylprednisolone

Product NDC: 49349-750
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: 49349-750
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040194
Marketing Category: ANDA
Start Marketing Date: 20120905

Package Information of Methylprednisolone

Package NDC: 49349-750-05
Package Description: 21 TABLET in 1 BLISTER PACK (49349-750-05)

NDC Information of Methylprednisolone

NDC Code 49349-750-05
Proprietary Name Methylprednisolone
Package Description 21 TABLET in 1 BLISTER PACK (49349-750-05)
Product NDC 49349-750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPREDNISOLONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120905
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name METHYLPREDNISOLONE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone


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