Hydralazine Hydrochloride Injection
Product Images NDC 70710-1988

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 70710-1988). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus 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

Image (35a2dca2 F3f1 4718 85b7 79597d6e7f43 01)

Image (35a2dca2 F3f1 4718 85b7 79597d6e7f43 01)
Chemical structure of Hydralazine Hydrochloride, showing the molecular arrangement of the active ingredient associated with the hydrazine and quinazoline components.*
FDA Label Image

Vial (35a2dca2 F3f1 4718 85b7 79597d6e7f43 02)

Vial (35a2dca2 F3f1 4718 85b7 79597d6e7f43 02)
Label for Hydralazine Hydrochloride Injection, USP 20 mg/mL in a 1 mL single-dose vial for intramuscular or intravenous use. The preservative-free product is distributed by Zydus Pharmaceuticals (USA) Inc. Storage instructions and a barcode are also shown on the label.*
FDA Label Image

Carton (35a2dca2 F3f1 4718 85b7 79597d6e7f43 03)

Carton (35a2dca2 F3f1 4718 85b7 79597d6e7f43 03)
Packaging label for Hydralazine Hydrochloride Injection, USP 20 mg/mL by Zydus Pharmaceuticals USA Inc. The label states it is for intramuscular or intravenous use, preservative-free, and comes in single-dose vials of 1 mL each, with 25 vials per package. Additional product information includes inactive ingredients, storage instructions, and barcodes.*

* 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.