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NDC 72266-0131-01 Voriconazole 10 mg/mL Details
Voriconazole 10 mg/mL
Voriconazole is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fosun Pharma USA Inc.. The primary component is VORICONAZOLE.
Product Information
| NDC | 72266-0131 |
|---|---|
| Product ID | 72266-131_f2792f5b-872a-2da9-e053-2995a90a3126 |
| Associated GPIs | 11407080002120 |
| GCN Sequence Number | 050444 |
| GCN Sequence Number Description | voriconazole VIAL 200 MG INTRAVEN |
| HIC3 | W3B |
| HIC3 Description | ANTIFUNGAL AGENTS |
| GCN | 17499 |
| HICL Sequence Number | 023720 |
| HICL Sequence Number Description | VORICONAZOLE |
| Brand/Generic | Generic |
| Proprietary Name | Voriconazole |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Voriconazole |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/mL |
| Substance Name | VORICONAZOLE |
| Labeler Name | Fosun Pharma USA Inc. |
| Pharmaceutical Class | Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA211099 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 72266-0131-01 (72266013101)
| NDC Package Code | 72266-131-01 |
|---|---|
| Billing NDC | 72266013101 |
| Package | 1 VIAL, SINGLE-DOSE in 1 CARTON (72266-131-01) / 20 mL in 1 VIAL, SINGLE-DOSE |
| Marketing Start Date | 2021-01-04 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |