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Methylprednisolone Sodium Succinate - 55390-258-01 - (Methylprednisolone Sodium Succinate)

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Drug Information of Methylprednisolone Sodium Succinate

Product NDC: 55390-258
Proprietary Name: Methylprednisolone Sodium Succinate
Non Proprietary Name: Methylprednisolone Sodium Succinate
Active Ingredient(s): 500    mg/8mL & nbsp;   Methylprednisolone Sodium Succinate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone Sodium Succinate

Product NDC: 55390-258
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040709
Marketing Category: ANDA
Start Marketing Date: 20080108

Package Information of Methylprednisolone Sodium Succinate

Package NDC: 55390-258-01
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (55390-258-01) > 8 mL in 1 VIAL, MULTI-DOSE

NDC Information of Methylprednisolone Sodium Succinate

NDC Code 55390-258-01
Proprietary Name Methylprednisolone Sodium Succinate
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (55390-258-01) > 8 mL in 1 VIAL, MULTI-DOSE
Product NDC 55390-258
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylprednisolone Sodium Succinate
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20080108
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
Strength Number 500
Strength Unit mg/8mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone Sodium Succinate


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