Hydroxyzine Hydrochloride Injection, Solution
Product Images NDC 0517-5601

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Hydroxyzine Hydrochloride (NDC 0517-5601). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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.

FDA Label Image

6e26bbb9-figure-01 (Hydroxyzine Hydrochloride Injection Usp 1)

Chemical structure of Hydroxyzine Hydrochloride showing its molecular formula C21H27ClN2O2·2HCl and molecular weight 447.83.*

FDA Label Image

Hydroxyzine Hydrochloride Injection Usp 10

Label for Hydroxyzine Hydrochloride containing a QR code, lot number 0000, expiration date 12/2018, GTIN 00305175602258, and serial number 100000000000. The label is from American Regent, Inc.*

FDA Label Image

1 mL (25 mg) Container Label (Hydroxyzine Hydrochloride Injection Usp 2)

Hydroxyzine Hydrochloride 25 mg/mL Injection, USP label for a 1 mL single dose vial. The label includes storage instructions to protect from light and store at 20° to 25°C (68° to 77°F). It is marked Rx Only and manufactured by American Regent, Inc., Shirley, NY.*

FDA Label Image

1 mL (25 mg) Carton (Hydroxyzine Hydrochloride Injection Usp 3)

Hydroxyzine Hydrochloride Injection, USP 25 mg/mL single dose vial label from American Regent, Inc. The label specifies intramuscular use only, with a package size of 25 vials of 1 mL each. It includes storage instructions, warnings, and barcode for product identification.*

FDA Label Image

1 mL (50 mg) Container Label (Hydroxyzine Hydrochloride Injection Usp 4)

Hydroxyzine Hydrochloride Injection, USP 50 mg/mL single-dose vial label. The label specifies 1 mL vial volume for intramuscular use only. It is a prescription-only product provided by American Regent, Inc., Shirley, NY. The label includes storage instructions to protect from light and keep at 20° to 25°C (68° to 77°F).*

FDA Label Image

1 mL (50 mg) Carton (Hydroxyzine Hydrochloride Injection Usp 5)

Hydroxyzine Hydrochloride Injection USP 50 mg/mL single dose vial label. Contains 25 vials of 1 mL each. For intramuscular use only. Manufactured by American Regent, Inc. Label includes storage instructions, warnings, active ingredient details, and barcode.*

FDA Label Image

2 mL Container Label (Hydroxyzine Hydrochloride Injection Usp 6)

Hydroxyzine Hydrochloride Injection, USP 100 mg/2 mL (50 mg/mL) single dose vial label by American Regent, Inc., specifying IM use only, Rx only. The label includes storage instructions to protect from light and store at 20° to 25°C (68° to 77°F) with directions to refer to the package insert. The label includes a barcode and lot/expiration fields.*

FDA Label Image

2 mL (50 mg) Carton (Hydroxyzine Hydrochloride Injection Usp 7)

Label for Hydroxyzine Hydrochloride Injection USP, 100 mg/2 mL (50 mg/mL), in single dose vials. The package contains 25 vials of 2 mL each. The label notes intramuscular use only, includes storage and handling instructions, and identifies American Regent, Inc. as the manufacturer.*

FDA Label Image

10 mL Container (Hydroxyzine Hydrochloride Injection Usp 8)

A data panel displaying a matrix barcode with accompanying product information including lot number (0000), expiration date (01/2099), GTIN (00305174201254), and serial number (0). This panel is likely part of the packaging for Hydroxyzine Hydrochloride by American Regent, Inc.*

FDA Label Image

10 mL Carton (Hydroxyzine Hydrochloride Injection Usp 9)

Packaging label featuring a Data Matrix barcode above printed text displaying lot number (0000), expiration date (01/2099), GTIN (00305175601251), and serial number (0). No proprietary or dosage information is visible on the label.*

* 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.