Hydralazine Hydrochloride Injection
Product Images NDC 55150-400

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hydralazine Hydrochloride (NDC 55150-400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

FDA Label Image

Package Label-principal Display Panel-20 mg Per mL (Container Label)

Package Label-principal Display Panel-20 mg Per mL (Container Label)
Label for HYDRALAZINE HYDROCHLORIDE Injection, USP 20 mg/mL single-dose vial for intramuscular or intravenous use. Manufactured in India for Eugia US LLC, stored at controlled room temperature. NDC 55150-400-01, 1 mL vial with instructions to discard unused portion.*
FDA Label Image

Package Label-principal Display Panel-20 mg Per mL (Container-Carton (25 Vials))

Package Label-principal Display Panel-20 mg Per mL (Container-Carton (25 Vials))
Packaging label for Hydralazine Hydrochloride Injection, USP 20 mg per mL by Eugia US LLC. It is intended for intramuscular or intravenous use and contains 25 single-dose vials of 1 mL each. The label includes product and strength information, usage route, storage instructions, inactive ingredients, and distributor details.*
FDA Label Image

Chemical Structure (Hydralazine HCl Str)

Chemical Structure (Hydralazine HCl Str)
Chemical structure of Hydralazine Hydrochloride depicted as a bicyclic compound with a phenyl ring attached to a hydrazine functional group and additional nitrogen atoms in the ring system.*

* 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.