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NDC 00143-9531-01 Ifosfamide 50 mg/mL Details
Ifosfamide 50 mg/mL
Ifosfamide is a INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is IFOSFAMIDE.
MedlinePlus Drug Summary
Ifosfamide is used in combination with other medications to treat cancer of the testicles that has not improved or that has worsened after treatment with other medications or radiation therapy. Ifosfamide is in a class of medications called alkylating agents. It works by slowing or stopping the growth of cancer cells in your body.
Related Packages: 00143-9531-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Ifosfamide Injection
Product Information
| NDC | 00143-9531 |
|---|---|
| Product ID | 0143-9531_0511e667-7034-446c-975b-3d48b77ad86d |
| Associated GPIs | 21101025002025 |
| GCN Sequence Number | 062946 |
| GCN Sequence Number Description | ifosfamide VIAL 1 G/20 ML INTRAVEN |
| HIC3 | V1A |
| HIC3 Description | ANTINEOPLASTIC - ALKYLATING AGENTS |
| GCN | 98709 |
| HICL Sequence Number | 004570 |
| HICL Sequence Number Description | IFOSFAMIDE |
| Brand/Generic | Generic |
| Proprietary Name | Ifosfamide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Ifosfamide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/mL |
| Substance Name | IFOSFAMIDE |
| Labeler Name | Hikma Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Alkylating Activity [MoA], Alkylating Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076619 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00143-9531-01 (00143953101)
| NDC Package Code | 0143-9531-01 |
|---|---|
| Billing NDC | 00143953101 |
| Package | 1 VIAL in 1 BOX (0143-9531-01) / 20 mL in 1 VIAL |
| Marketing Start Date | 2017-06-10 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |