Structural Formula (Ondansetron Injection Usp 1)
Ondansetron Injection
Product Images NDC 0641-6079
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Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 0641-6079). 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.
Product Images & Figures Index
Ondansetron Injection, Usp 4 mg/2 mL (2 mg/ml) 2 mL Single Dose Vial (Ondansetron Injection Usp 2)
This is the label of an Ondansetron Injection, USP, which is used for IV or IM injection. Each 2 mL of this solution contains 4 mg of Ondansetron. It comes in a 2L single-dose vial and should be protected from light. The batch or the lot number mentioned on the label is "NDG 0641607801 oty" and the code is "on000s1007s0Te".*
Ondansetron Injection, Usp 4 mg/2 mL (2 mg/ml) 25 X 2 mL Single Dose Vials (Ondansetron Injection Usp 3)
This is a prescription-only medication called Ondansetron. It comes in single dose vials containing 4mg per 2 mL for intravenous or intramuscular injection. It is light sensitive and should be kept in the carton until use. The solution is sterile and contains ondansetron 2mg and other components as buffers. Dosage and administration instructions are available in the package insert. The medication should be stored at room temperature and protected from light. This information is provided by Hikma Pharmaceuticals.*
Ondansetron Injection, Usp 40 mg/20 mL (2 mg/ml) 20 mL Multiple Dose Vial (Ondansetron Injection Usp 4)
This is an intravenous or intramuscular injection medication called Ondansetron. It is supplied in a 20 mL multiple-dose vial, with each mL containing 2 mg of ondansetron hydrochloride dihydrate, 8.3 mg sodium chloride, 0.5 mg citric acid monohydrate, and 0.25 mg sodium citrate dihydrate as buffers, as well as 1.2 mg methylparaben and 0.15 mg propylparaben as preservatives. The package insert should be consulted for dosage and administration instructions. The medication should be stored at 20°C to 25°C (68°F to 77°F) and protected from light. It is manufactured by Hikma in Berkeley Heights, NJ.*
Ondansetron Injection, Usp 40 mg/20 mL (2 mg/ml) 20 mL Multiple Dose Vial (Ondansetron Injection Usp 5)
This is a description of a medication called Ondansetron. It is available in an injection form either for intravenous or intramuscular use. The medication comes in a 20 mL multi-dose vial with a concentration of 40 mg per 20 mL. The NDC numbers for this medication are 0641-6079-01 and 0641-6079-01.*
Ondansetron Injection Usp 6
This is a product description with a GTIN (Global Trade Item Number), SN (Serial Number), EXP (Expiration Date), and LOT (Lot Number). The GTIN is 0301234567896, the SN is 1234567890123, the EXP is in MMMYYYY format, and the LOT is ABCDE12345.*
Ondansetron Injection Usp 7
This text provides information that seems to be related to product or inventory management. There is a "Lot" identified as "ABCDET2345" and an "EXp" marked "HHRYYYY". Additionally, there is a Global Trade Identification Number (GTIN) with the value "0301234567896". There's also a serial number (SN) with the value "12345678901234". The purpose of this text is not entirely clear without additional context.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
