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Myochrysine - 17478-533-10 - (Gold Sodium Thiomalate)

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Drug Information of Myochrysine

Product NDC: 17478-533
Proprietary Name: Myochrysine
Non Proprietary Name: Gold Sodium Thiomalate
Active Ingredient(s): 50    mg/mL & nbsp;   Gold Sodium Thiomalate
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Myochrysine

Product NDC: 17478-533
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100422

Package Information of Myochrysine

Package NDC: 17478-533-10
Package Description: 1 VIAL in 1 CARTON (17478-533-10) > 10 mL in 1 VIAL

NDC Information of Myochrysine

NDC Code 17478-533-10
Proprietary Name Myochrysine
Package Description 1 VIAL in 1 CARTON (17478-533-10) > 10 mL in 1 VIAL
Product NDC 17478-533
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Gold Sodium Thiomalate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 20100422
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Akorn, Inc.
Substance Name GOLD SODIUM THIOMALATE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient]

Complete Information of Myochrysine


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