Benazepril Hydrochloride Tablet
Product Images NDC 23155-752

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Benazepril Hydrochloride (NDC 23155-752). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet 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

Image (12e1c649 115a 4141 8ff8 A1d6755799dd 01)

Chemical structure of Benazepril Hydrochloride depicting its molecular framework, including aromatic rings, amide, and carboxyl groups, consistent with the active ingredient in the product.*

FDA Label Image

Image (12e1c649 115a 4141 8ff8 A1d6755799dd 02)

FDA Label Image

Container-label-5 mg (12e1c649 115a 4141 8ff8 A1d6755799dd 03)

Benazepril Hydrochloride Tablets, USP 5 mg oral tablets, 100 count package by Avet Pharmaceuticals Inc. The label indicates prescription use only and includes handling instructions such as storage temperature (20° to 25°C), protection from moisture, and to keep out of reach of children.*

FDA Label Image

Label-5mg (Benazepril 5 mg)

Label for Benazepril Hydrochloride Tablets USP 5 mg, oral tablet form, supplied in a package of 100 tablets. The label is branded as Avet Pharma by Heritage Pharmaceuticals Inc. It includes storage instructions, dosage form, and manufacturer information, with a clear display of the NDC number 23155-749-01 and a barcode.*

FDA Label Image

Container-label-10 mg (12e1c649 115a 4141 8ff8 A1d6755799dd 04)

Benazepril Hydrochloride Tablets, USP 10 mg, oral tablets in a 100-count package. The label includes dosage strength, quantity, and manufacturer information for Avet Pharmaceuticals Inc., a division of Heritage Pharmaceuticals. It also contains storage instructions, warnings, and a barcode.*

FDA Label Image

Label-10mg (Benazepril 10 mg)

Label for Benazepril Hydrochloride Tablets USP, 10 mg strength, in a package containing 100 tablets. The label shows the product name, dosage strength, quantity, and designation as prescription-only. It also includes storage instructions, manufacturer details (Avet Pharmaceuticals Inc.), a barcode, and the revision date of 08/2023. The label design uses blue and red text on a white background.*

FDA Label Image

Container-label-20 mg (12e1c649 115a 4141 8ff8 A1d6755799dd 05)

Label for Benazepril Hydrochloride Tablets, USP 20 mg by Avet Pharma. The package contains 100 oral tablets. The label includes dosage information, storage instructions, manufacturer details (Avet Pharmaceuticals Inc.), and a barcode. The note "NO VARNISH" is printed on the side.*

FDA Label Image

Label-20mg (Benazepril 20 mg)

Benazepril Hydrochloride Tablets USP 20 mg oral tablet label showing 100 tablets per container. The label includes NDC 23155-751-01, manufacturer Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., storage instructions, and barcodes. The label also states 'NO VARNISH 38 x 25 mm'.*

FDA Label Image

Container-label-40 mg (12e1c649 115a 4141 8ff8 A1d6755799dd 06)

Label for Benazepril Hydrochloride Tablets, USP 40 mg by Avet Pharma. The package contains 100 tablets for oral use. The label includes storage instructions, a barcode, and states that the product is available by prescription only.*

FDA Label Image

Label-40mg (Benazepril 40 mg)

Label for Benazepril Hydrochloride Tablets, USP, 40 mg strength, oral tablet dosage form. The bottle contains 100 tablets and is for prescription use only. The label shows Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. as the labeler. It includes storage instructions, USP references, a barcode, and a notice to keep out of reach of children.*

* 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.