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A-METHAPRED - 0409-3217-15 - (METHYLPREDNISOLONE SODIUM SUCCINATE)

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Drug Information of A-METHAPRED

Product NDC: 0409-3217
Proprietary Name: A-METHAPRED
Non Proprietary Name: METHYLPREDNISOLONE SODIUM SUCCINATE
Active Ingredient(s): 40    mg/mL & 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 A-METHAPRED

Product NDC: 0409-3217
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040664
Marketing Category: ANDA
Start Marketing Date: 20120221

Package Information of A-METHAPRED

Package NDC: 0409-3217-15
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3217-15) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of A-METHAPRED

NDC Code 0409-3217-15
Proprietary Name A-METHAPRED
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-3217-15) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-3217
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 20120221
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name METHYLPREDNISOLONE SODIUM SUCCINATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of A-METHAPRED


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