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NDC 00049-0114-28 ERAXIS 50 mg/15mL Details
ERAXIS 50 mg/15mL
ERAXIS is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Roerig. The primary component is ANIDULAFUNGIN.
Product Information
NDC | 00049-0114 |
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Product ID | 0049-0114_fa6cff94-4d7e-4240-b7e1-7fd3e573ed47 |
Associated GPIs | 11500010002120 |
GCN Sequence Number | 060436 |
GCN Sequence Number Description | anidulafungin VIAL 50 MG INTRAVEN |
HIC3 | W3A |
HIC3 Description | ANTIFUNGAL ANTIBIOTICS |
GCN | 26594 |
HICL Sequence Number | 033502 |
HICL Sequence Number Description | ANIDULAFUNGIN |
Brand/Generic | Brand |
Proprietary Name | ERAXIS |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | anidulafungin |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route | INTRAVENOUS |
Active Ingredient Strength | 50 |
Active Ingredient Units | mg/15mL |
Substance Name | ANIDULAFUNGIN |
Labeler Name | Roerig |
Pharmaceutical Class | Echinocandin Antifungal [EPC], Lipopeptides [CS] |
DEA Schedule | n/a |
Marketing Category | NDA |
Application Number | NDA021632 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00049-0114-28 (00049011428)
NDC Package Code | 0049-0114-28 |
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Billing NDC | 00049011428 |
Package | 15 mL in 1 VIAL, SINGLE-USE (0049-0114-28) |
Marketing Start Date | 2006-02-17 |
NDC Exclude Flag | N |
Pricing Information | N/A |