Product Images Granisetron Hydrochloride
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Product Label Images
The following 7 images provide visual information about the product associated with Granisetron Hydrochloride NDC 0143-9744 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.
This is a description of a medication named Granisetron Hydrochloride Injection, USP. It comes in a single dose vial of 1 mg/mL concentration and is intended for intravenous use. The vial should be stored between 15°C and 30°C (59°F and 86°F) in a controlled environment according to USP standards. The product is only available with a prescription (Rx only).*
This is a description of a medication called Granisetron Hydrochloride Injection. The medication is for intravenous use only and is available in 101 ml single dose vials with a concentration of 1 mg/mL. The manufacturer is Hikma and the National Drug Code (NDC) number is 0143-9744-10.*
This is a prescription drug with National Drug Code (NDC) 0143-9745-01 indicated only for intravenous use. It is a vial of Granisetron E Hydrochloride Injection, USP with a volume of 4ml. The package insert recommends protecting the drug from light. The lot and expiration date are indicated but not provided in the text.*
This is a description of an injectable medicine called Granisetron Hydrochloride. It is supplied in 5 multiple-dose vials, with each vial containing 4 mg per 4 mL, with 1 mg of Granisetron Hydrochloride per mL. The medicine is meant for intravenous use only and is available by prescription. The manufacturer is Hikma.*
This is a description of a medication called Granisetron Hydrochloride Injection, USP. It is available in multiple dose vials containing 4mg of medication per 4mL of solution, with a concentration of 1mg/mL. It is designed for intravenous use only and is identified by the NDC codes: 0143-9745-10 Rxonly and NDC 0143-9745-10 PRxonly. The manufacturer of this medication is Hikma Pharmaceuticals.*
This is a product identification label containing the GTIN (Global Trade Item Number), serial number (SN), expiration date (EXP), and lot number (LOT) of a product. However, the specific product or industry cannot be determined from this information alone.*
* 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.