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Methylprednisolone - 49999-153-21 - (methylprednisolone)

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Drug Information of Methylprednisolone

Product NDC: 49999-153
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: 49999-153
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011153
Marketing Category: NDA
Start Marketing Date: 20120209

Package Information of Methylprednisolone

Package NDC: 49999-153-21
Package Description: 21 TABLET in 1 DOSE PACK (49999-153-21)

NDC Information of Methylprednisolone

NDC Code 49999-153-21
Proprietary Name Methylprednisolone
Package Description 21 TABLET in 1 DOSE PACK (49999-153-21)
Product NDC 49999-153
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methylprednisolone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120209
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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