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Methylprednisolone Sodium Succinate - 63323-265-30 - (METHYLPREDNISOLONE SODIUM SUCCINATE)

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Drug Information of Methylprednisolone Sodium Succinate

Product NDC: 63323-265
Proprietary Name: Methylprednisolone Sodium Succinate
Non Proprietary Name: METHYLPREDNISOLONE SODIUM SUCCINATE
Active Ingredient(s): 1    g/16mL & 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: 63323-265
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040612
Marketing Category: ANDA
Start Marketing Date: 20041130

Package Information of Methylprednisolone Sodium Succinate

Package NDC: 63323-265-30
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) > 16 mL in 1 VIAL, MULTI-DOSE

NDC Information of Methylprednisolone Sodium Succinate

NDC Code 63323-265-30
Proprietary Name Methylprednisolone Sodium Succinate
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (63323-265-30) > 16 mL in 1 VIAL, MULTI-DOSE
Product NDC 63323-265
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 20041130
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
Strength Number 1
Strength Unit g/16mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone Sodium Succinate


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