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NDC 70710-1725-06 Micafungin 20 mg/mL Details
Micafungin 20 mg/mL
Micafungin is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is MICAFUNGIN SODIUM.
Product Information
| NDC | 70710-1725 |
|---|---|
| Product ID | 70710-1725_fe33b956-b91b-4b63-856d-544e6cb1c250 |
| Associated GPIs | |
| GCN Sequence Number | 061686 |
| GCN Sequence Number Description | micafungin sodium VIAL 100 MG INTRAVEN |
| HIC3 | W3A |
| HIC3 Description | ANTIFUNGAL ANTIBIOTICS |
| GCN | 97472 |
| HICL Sequence Number | 032804 |
| HICL Sequence Number Description | MICAFUNGIN SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Micafungin |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Micafungin |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/mL |
| Substance Name | MICAFUNGIN SODIUM |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Echinocandin Antifungal [EPC], Lipopeptides [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA215241 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1725-06 (70710172506)
| NDC Package Code | 70710-1725-6 |
|---|---|
| Billing NDC | 70710172506 |
| Package | 10 VIAL in 1 CARTON (70710-1725-6) / 5 mL in 1 VIAL (70710-1725-1) |
| Marketing Start Date | 2023-04-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |