Benazepril Hydrochloride Tablet, Coated
Product Images NDC 43547-336

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride (NDC 43547-336). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare U.s., 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

Structure (Bb91223e Ffa5 4a3a B191 Fe121250c20c 01)

Chemical structure of Benazepril Hydrochloride, showing its molecular components, including aromatic rings, carbon chains, and functional groups characteristic of the compound.*

FDA Label Image

Container Label 5 mg (Bb91223e Ffa5 4a3a B191 Fe121250c20c 02)

Label for Benazepril Hydrochloride Tablets, USP 5 mg, coated oral tablets. The package contains 100 tablets. Labeler is Solco Healthcare U.S., LLC. Includes storage instructions, dosage advisory, manufacturer and distributor information, NDC 43547-335-10, and a barcode.*

FDA Label Image

Bb91223e Ffa5 4a3a B191 Fe121250c20c 03

Label for Benazepril Hydrochloride Tablets, USP 10 mg, coated oral tablets, packaged as 100 tablets. The label includes the NDC 43547-336-10 and indicates prescription use only. Manufactured by Zhejiang Huahai Pharmaceutical Co., Ltd., China, and distributed by Solco Healthcare U.S., LLC, Somerset, NJ. Storage instructions and warnings about keeping out of reach of children are also present.*

FDA Label Image

Container Label 20 mg 100 Ct (Bb91223e Ffa5 4a3a B191 Fe121250c20c 04)

Label for Benazepril Hydrochloride Tablets USP, 20 mg, oral coated tablets. The label indicates a package size of 100 tablets. It includes storage instructions, manufacturer Zhejiang Huahai Pharmaceutical Co., Ltd. in China, and distributor Solco Healthcare US, LLC. The NDC number is 43547-337-10, and the product is for prescription use only.*

FDA Label Image

Container Label 40 mg 100 Ct (Bb91223e Ffa5 4a3a B191 Fe121250c20c 05)

Label for Benazepril Hydrochloride tablets USP, 40 mg strength, in a package of 100 tablets. The label indicates prescription use only and includes storage instructions and manufacturer details. The labeler is Solco Healthcare U.S., LLC.*

FDA Label Image

Container Label 10 mg (Image 01)

Label for Benazepril Hydrochloride Tablets, USP 5 mg by Solco Healthcare U.S., LLC. The label displays the product name, strength (5 mg), dosage form as coated tablets, and package count of 100 tablets. It includes storage instructions, manufacturer details (Prinston Laboratories), a barcode, and a note about a non-coating area measuring 15.5 mm by 29 mm.*

FDA Label Image

Container Label 40 mg 30 Ct (Image 02)

Label for Benazepril Hydrochloride Tablets, USP 10 mg, coated oral tablets. The package contains 100 tablets and is labeled for prescription use only. Manufactured by Prinston Laboratories and distributed by Solco Healthcare U.S., LLC. Storage instructions specify keeping the container at 20-25°C (68-77°F) and protecting from moisture. Includes NDC number 43547-336-10 and barcode.*

FDA Label Image

Container Label 20 mg 30 Ct (Image 03)

Benazepril Hydrochloride 20 mg coated tablets, USP, bottle label showing 100 tablets, labeled for oral use. The label includes dosage strength, NDC 43547-337-10, manufacturer Solco Healthcare U.S., LLC, and storage instructions. The label also displays a barcode and a note indicating the tablet non-coating area size.*

FDA Label Image

Image 04

Label for Benazepril Hydrochloride Tablets, USP 40 mg, coated oral tablets. The package contains 100 tablets. The label includes manufacturer information for Solco Healthcare U.S., LLC, and distributor details. Dosage and storage instructions are partially visible, as well as a barcode and NDC 43547-338-10.*

* 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.