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