Granisetron Hydrochloride Injection
Product Images NDC 0143-9744

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Granisetron Hydrochloride (NDC 0143-9744). 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.*

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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.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.