Hydralazine Hydrochloride Injection, Solution
Product Images NDC 0641-6231

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hydralazine Hydrochloride (NDC 0641-6231). 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.

FDA Label Image

Structure Thb Size (Hydralazine Hydrochloride Injection 1)

Chemical structure diagram of Hydralazine hydrochloride, showing a bicyclic ring system with nitrogen atoms and an attached hydrazine group, along with the hydrochloride component.*

FDA Label Image

462-903-00 (Hydralazine Hydrochloride Injection 2)

Label for HydrALAZINE Hydrochloride Injection, USP, 20 mg/mL solution for intramuscular or intravenous use. The label indicates prescription status, preservative-free composition, and a warning to discard unused portions. Manufactured by Hikma Pharmaceuticals USA Inc. Features a barcode, lot number, and expiration date fields.*

FDA Label Image

462-904-00 (Hydralazine Hydrochloride Injection 3)

Label for HydrALAZINE Hydrochloride Injection, USP 20 mg/mL solution for injection, intended for intramuscular or intravenous use. The preservative-free product is supplied in 25 single-dose 1 mL vials. Manufactured by Hikma Pharmaceuticals USA Inc., with storage instructions and usage warnings noted.*

FDA Label Image

Layout 1 Resized (Hydralazine Hydrochloride Injection 4)

Label for HydrALAZINE hydrochloride injection, solution, showing batch information including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The label is from Hikma Pharmaceuticals USA Inc., for the 20 mg/mL strength.*

* 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.