Product Images Irinotecan Hydrochloride

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Product Label Images

The following 8 images provide visual information about the product associated with Irinotecan Hydrochloride NDC 0143-9701 by Hikma Pharmaceuticals Usa Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Chemical structure - irinotecan hydrochloride injection 1

Figure 1. Survival Second-Line Irinotecan vs Best Supportive Care (BSC) Study 7 - irinotecan hydrochloride injection 2

Figure 2. Survival Second-Line Irinotecan vs Infusion 5-FU Study 8 - irinotecan hydrochloride injection 3

NDC 0143-9702-01 IRINOTECAN HYDROCHLORIDE INJECTION, USP 40 mg/2 mL (20 mg/mL) as the trihydrate MUST BE DILUTED - CYTOTOXIC AGENT FOR IV USE ONLY Rx ONLY 2 mL Single Dose Vial USUAL DOSAGE: See package insert. PROTECT FROM LIGHT. PROTECT FROM FREEZING. Store at 20º to 25ºC (68º to 77ºF); excursions permitted to 15º to 30ºC (59º to 86ºF) [See USP Controlled Room Temperature]. - irinotecan hydrochloride injection 4

This is a product label for Irinotecan HCI Injection, USP containing 40mg per 2mL, to be used for intravenous purposes only. The product code is NDC0143.9702-01 and the drug should be administered under the direction of a healthcare professional.*

NDC 0143-9702-01 1 x 2 mL Single Dose Vial IRINOTECAN HYDROCHLORIDE INJECTION, USP 40 mg/2 mL (20 mg/mL)* as the trihydrate MUST BE DILUTED - CYTOTOXIC AGENT FOR IV USE ONLY Rx ONLY - irinotecan hydrochloride injection 5

This text refers to a medication called Irinotecan Hydrochloride Injection, which is a cytotoxic agent used for intravenous administration only. The package contains a 2mL single dose vial. The medication must be diluted before use, and it is important to protect it from light and at room temperature. The dosage information is available on the package's instructions. The text also includes some technical information about the medication, such as its chemical components and NDC code.*

NDC 0143-9701-01 IRINOTECAN HYDROCHLORIDE INJECTION, USP 100 mg/5 mL (20 mg/mL) as the trihydrate MUST BE DILUTED - CYTOTOXIC AGENT FOR IV USE ONLY Rx ONLY 5 mL Single Dose Vial USUAL DOSAGE: See package insert. PROTECT FROM LIGHT. PROTECT FROM FREEZING. Store at 20º to 25ºC (68º to 77ºF); excursions permitted to 15º to 30ºC (59º to 86ºF) [See USP Controlled Room Temperature]. - irinotecan hydrochloride injection 6

This appears to be a label for the medication Irinotecan, specifically for the injection form, with a concentration of 20mg/mL. The NDC number is listed as 01430101, and the label states that it is for intravenous use only.*

NDC 0143-9701-01 1 x 5 mL Single Dose Vial IRINOTECAN HYDROCHLORIDE INJECTION, USP 100 mg/5 mL (20 mg/mL)* as the trihydrate MUST BE DILUTED - CYTOTOXIC AGENT FOR IV USE ONLY Rx ONLY - irinotecan hydrochloride injection 7

irinotecan hydrochloride injection 8

This text provides product identification and expiration details. The GTIN code, 0301234567896, is a globally recognized product identification code. The SN, 1234567890123, is likely a unique serial number. The EXP date, indicated as MMMYYYY, is the expiration date of the product. Lastly, the LOT code, ABCDE12345, may signify a batch or lot number for production and tracking purposes.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.