Benazepril Hydrochloride And Hydrochlorothiazide Tablet
Product Images NDC 62559-417

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride And Hydrochlorothiazide (NDC 62559-417). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Benazepril-structure.jpg (Image 01)

Chemical structure of Benazepril Hydrochloride, showing its molecular configuration including key functional groups and the hydrochloride component.*

FDA Label Image

Hydrochlorothiazide-structure.jpg (Image 02)

Chemical structure diagram of benazepril hydrochloride showing its molecular framework including aromatic ring, sulfonamide, chlorine, and other functional groups.*

FDA Label Image

Ani-logo (Image 03)

FDA Label Image

5mg-6.25mg Label (Image 04)

Label for Benazepril Hydrochloride and Hydrochlorothiazide Tablets USP 5 mg/6.25 mg, oral tablets in a bottle of 100. The label includes active ingredient strengths, storage instructions, warnings to keep out of reach of children, and is manufactured by ANI Pharmaceuticals, Inc. The label also shows an NDC code and barcode.*

FDA Label Image

10mg-12.5mg Label (Image 05)

Label for Benazepril Hydrochloride and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg strength. The label indicates the product contains 100 tablets, manufactured by ANI Pharmaceuticals, Inc. The label includes storage instructions, dosage guidance note, warnings to keep out of reach of children, and the NDC number 62559-415-01. A barcode and other identification codes are also visible.*

FDA Label Image

20mg-12.5mg Label (Image 06)

Label for Benazepril Hydrochloride and Hydrochlorothiazide Tablets USP, with strengths of 20 mg and 12.5 mg respectively. The label states the product is prescription-only (Rx only) and contains 100 tablets. It includes storage instructions, manufacturer ANI Pharmaceuticals, Inc., and a barcode with corresponding NDC 62559-416-01.*

FDA Label Image

20mg-25mg Label (Image 07)

Label for Benazepril Hydrochloride and Hydrochlorothiazide Tablets USP, 20 mg/25 mg, oral tablets. The package contains 100 tablets. Manufactured by ANI Pharmaceuticals, Inc., Baudette, MN. The label includes dosage information, storage instructions, and a barcode.*

* 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.