Hydralazine Hydrochloride Injection, Solution
Product Images NDC 72572-265

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Hydralazine Hydrochloride (NDC 72572-265). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Adobe Systems (Hydralazine Hydrochloride Injection 1)

Chemical structure diagram of Hydralazine Hydrochloride showing its molecular framework including the hydrazine group attached to a fused bicyclic ring system, along with the hydrochloride component represented separately.*

FDA Label Image

Civica Logo (Hydralazine Hydrochloride Injection 2)

FDA Label Image

Container Label (Civica)

Label for Hydralazine Hydrochloride Injection, USP 20 mg/mL by Civica, Inc. The label indicates a 1 mL single dose ampule for intramuscular or intravenous use. It includes storage instructions at 20°-25°C, warnings about discarding unused portions, a barcode, lot and expiration date fields, and the NDC 72572-265-01.*

FDA Label Image

Carton Labeling (Civica)

Label for Hydralazine Hydrochloride Injection, USP 20 mg/mL, a solution for intramuscular or intravenous use. The label indicates packaging of 25 single-dose vials, each 1 mL, manufactured by Civica, Inc. and American Regent, Inc. Dosage form and storage instructions are included alongside the NDC 72572-265-25 and Rx only designation.*

FDA Label Image

Serialization Label (Civica)

Label panel displaying lot number, expiration date (November 2020), GTIN code, and serial number for Hydralazine Hydrochloride injection, solution, 20 mg/mL by Civica, Inc. The label includes a small QR code.*

* 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.