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NDC 55150-0392-01 BENDAMUSTINE HYDROCHLORIDE 100 mg/20mL Details
BENDAMUSTINE HYDROCHLORIDE 100 mg/20mL
BENDAMUSTINE HYDROCHLORIDE is a INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eugia US LLC. The primary component is BENDAMUSTINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Bendamustine injection is used to treat chronic lymphocytic leukemia (CLL; a type of cancer of the white blood cells). Bendamustine injection is also used to treat a type of non-Hodgkins lymphoma (NHL: cancer that begins in a type of white blood cell that normally fights infection) that is slow spreading, but has continued to worsen during or after treatment with another medication. Bendamustine is in a class of medications called alkylating agents. It works by killing existing cancer cells and limiting the growth of new cancer cells.
Related Packages: 55150-0392-01Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Bendamustine Injection
Product Information
| NDC | 55150-0392 |
|---|---|
| Product ID | 55150-392_4357b1f0-fcc2-448a-9580-13b55ba470de |
| Associated GPIs | |
| GCN Sequence Number | 042496 |
| GCN Sequence Number Description | bendamustine HCl VIAL 100 MG INTRAVEN |
| HIC3 | V1A |
| HIC3 Description | ANTINEOPLASTIC - ALKYLATING AGENTS |
| GCN | 12014 |
| HICL Sequence Number | 016785 |
| HICL Sequence Number Description | BENDAMUSTINE HCL |
| Brand/Generic | Generic |
| Proprietary Name | BENDAMUSTINE HYDROCHLORIDE |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BENDAMUSTINE HYDROCHLORIDE |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route | INTRAVENOUS |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/20mL |
| Substance Name | BENDAMUSTINE HYDROCHLORIDE |
| Labeler Name | Eugia US LLC |
| Pharmaceutical Class | Alkylating Activity [MoA], Alkylating Drug [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA214739 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 55150-0392-01 (55150039201)
| NDC Package Code | 55150-392-01 |
|---|---|
| Billing NDC | 55150039201 |
| Package | 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-392-01) / 20 mL in 1 VIAL, SINGLE-DOSE |
| Marketing Start Date | 2023-06-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |