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MYCAMINE
MYCAMINE - 0469-3250-10 - (micafungin sodium)
Drug Information of MYCAMINE
| Product NDC: | 0469-3250 |
| Proprietary Name: | MYCAMINE |
| Non Proprietary Name: | micafungin sodium |
| Active Ingredient(s): | 10 mg/mL & nbsp; micafungin sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MYCAMINE
| Product NDC: | 0469-3250 |
| Labeler Name: | Astellas Pharma US, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021506 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050316 |
Package Information of MYCAMINE
| Package NDC: | 0469-3250-10 |
| Package Description: | 10 VIAL, SINGLE-USE in 1 CARTON (0469-3250-10) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Information of MYCAMINE
| NDC Code | 0469-3250-10 |
| Proprietary Name | MYCAMINE |
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (0469-3250-10) > 5 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0469-3250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | micafungin sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050316 |
| Marketing Category Name | NDA |
| Labeler Name | Astellas Pharma US, Inc. |
| Substance Name | MICAFUNGIN SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Echinocandin Antifungal [EPC],Lipopeptides [Chemical/Ingredient] |
