Hydralazine Hydrochloride Tablet
Product Images NDC 55154-5689

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 55154-5689). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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.

FDA Label Image

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B7b326f9 9466 4882 Bd37 2751631edc79 00
Label for Hydralazine Hydrochloride Tablets USP 50 mg, containing 10 tablets. The label includes dosage information, storage conditions, and warnings. It notes the product is manufactured by Teva Czech Industries in the Czech Republic and distributed by Mylan Institutional Inc. and Cardinal Health. The label includes an NDC barcode and batch number B60.*
FDA Label Image

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B7b326f9 9466 4882 Bd37 2751631edc79 01
Label of Hydralazine Hydrochloride Tablets USP 25 mg, oral dosage form, with a package count of 10 tablets. The label includes storage instructions at controlled room temperature, a warning about the unit dose package not being child resistant and intended for institutional use only. Manufactured by Teva Czech Industries in the Czech Republic and distributed by Mylan Institutional Inc. and Cardinal Health.*
FDA Label Image

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Hydralazine Hydrochloride Tablet 089097 088467 088 1
Chemical structure diagram of Hydralazine Hydrochloride, showing the fused bicyclic ring system with attached hydrazine and hydrochloride groups as part of the molecular structure.*

* 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.