Granisetron Hydrochloride Injection
Product Images NDC 0143-9745

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Granisetron Hydrochloride (NDC 0143-9745). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Granisetron HCl Injection 1)

Description not available.*

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1 mg Vial (Granisetron HCl Injection 2)

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).*

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1 mg Carton (Granisetron HCl Injection 3)

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.*

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4 mg Vial (Granisetron HCl Injection 4)

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.*

FDA Label Image

Ndc 0143-9745-10 10 X 4 mL Multi-use Vials Granisetron Hydrochloride Injection, Usp 4 mg/4 mL (1 mg/ml*) For Intravenous Use Only Rx Only *each mL Contains, In Sterile Aqueous Solution, Granisetron Hydrochloride, Usp, 1.12 mg, Equivalent To Gransietron, 1 mg, Sodium Chloride, Usp, 9 mg, Citric Acid, Nf, 2 mg, Benzyl Alcohol, Nf, 10 mg, As A Preservative. Ph Adjusted With Sodium Hydroxide/ Hydrochloric Acid. Usual Dosage: See Package Insert. Store At 20º To 25ºc (68º To 77ºf); Excursions Permitted To 15º To 30ºc (59º To 86ºf) [see Usp Controlled Room Temperature]. Do Not Freeze. Protect From Light. Retain In Carton Until Time Of Use. (Granisetron HCl Injection 5)

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.*

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Granisetron HCl Injection 6

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.*

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Granisetron HCl Injection 7

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.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.