Ondansetron Injection
Product Images NDC 0143-9890

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 0143-9890). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

FDA Label Image

Structural Formula (Ondansetron Injection 1)

FDA Label Image

Ndc 0143-9891-01 Ondansetron Injection, Usp 4 mg/2 mL (2 mg/ml) Sterile For Iv Or Im Use Rx Only 2 mL Single Dose Vial Usual Dosage: See Package Insert. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. Protect From Light. (Ondansetron Injection 2)

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Ndc 0143-9890-01 Ondansetron Injection, Usp 40 mg/20 mL (2 mg/ml) Sterile For Iv Or Im Use Rx Only 20 mL Multiple Dose Vial Each 1 mL Of Aqueous Solution In The 20 mL Multidose Vial Contains 2 mg Of Ondansetron As The Hydrochloride Dihydrate; 8.3 mg Of Sodium Chloride, Usp; 0.5 mg Of Citric Acid Monohydrate, Usp And 0.25 mg Trisodium Citrate Dihydrate, Usp As Buffers; And 1.2 mg Of Methylparaben, Nf And 0.15 mg Of Propylparaben As Preservatives In Water For Injection, Usp. Usual Dosage: See Package Insert. Store At 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. Protect From Light. (Ondansetron Injection 3)

This is a description of a medication called Ondansetron, which comes in an injection form. The medication contains 40mg/20mL (2 my/ml) and is suitable for intravenous or intramuscular use. The medication is sterile and contains 8.3 m Sodium Chloride, USP. The recommended dosage can be found on the package and it is stored under controlled temperature and pressure. The medication is distributed by WESTWARD PHARMACEUTICAL CORF. and is from a Lot number that is not provided.*

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Ndc 0143-9890-10 Rx Only Ondansetron Injection, Usp 40 mg/20 mL (2 mg/ml) Sterile For Iv Or Im Administration 10 X 20 mL Multiple Dose Vials Each 1 mL Of Aqueous Solution In The 20 mL Multiple Dose Vial Contains 2 mg Of Ondansetron As The Hydrochloride Dihydrate; 8.3 mg Sodium Chloride, Usp; 0.5 mg Of Citric Acid Monohydrate, Usp And 0.25 mg Trisodium Citrate Dihydrate, Usp As Buffers; And 1.2 mg Of Methylparaben, Nf And 0.15 mg Of Propylparaben As Preservatives In Water For Injection, Usp. Usual Dosage: See Package Insert. Store Between 20º To 25ºc (68º To 77ºf) [see Usp Controlled Room Temperature]. Protect From Light. (Ondansetron Injection 4)

This is a product description for Ondansetron injection, USP. It comes in a 40 mg/20mL dosage vial for intravenous or intramuscular administration. Each 1 mL of the solution contains 2 mg of ondansetron and other ingredients. The product should be stored at a controlled room temperature between 20 and 25 degrees Celsius. The dosage is indicated in the package. It is distributed by West-Ward in Estertown, NJ.*

FDA Label Image

Ondansetron Injection 5

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