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MethylpredniSOLONE - 51991-188-01 - (METHYLPREDNISOLONE)

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Drug Information of MethylpredniSOLONE

Product NDC: 51991-188
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: 51991-188
Labeler Name: Breckenridge Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040189
Marketing Category: ANDA
Start Marketing Date: 20031107

Package Information of MethylpredniSOLONE

Package NDC: 51991-188-01
Package Description: 100 TABLET in 1 BOTTLE (51991-188-01)

NDC Information of MethylpredniSOLONE

NDC Code 51991-188-01
Proprietary Name MethylpredniSOLONE
Package Description 100 TABLET in 1 BOTTLE (51991-188-01)
Product NDC 51991-188
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHYLPREDNISOLONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031107
Marketing Category Name ANDA
Labeler Name Breckenridge Pharmaceutical, 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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