Amlodipine Besylate And Benazepril Hydrochloride Capsule
Product Images NDC 71335-2634

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate And Benazepril Hydrochloride (NDC 71335-2634). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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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Chemical structure diagram of Benazepril Hydrochloride, one of the active ingredients in Amlodipine Besylate and Benazepril Hydrochloride capsules. The structure shows molecular bonds and functional groups characteristic of benazepril with an attached HCl moiety.*

FDA Label Image

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Chemical structure of Amlodipine Besylate showing molecular groups including a chlorophenyl ring, methoxyethyl amine side chain, and a benzenesulfonic acid moiety representing the besylate component.*

FDA Label Image

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A rectangular carton package for Amlodipine Besylate and Benazepril Hydrochloride capsules. The label indicates a strength of 5 mg and 10 mg for the active ingredients respectively. The package is manufactured by Bryant Ranch Prepack. The design includes a white background with black text and a barcode on the bottom section.*

FDA Label Image

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A prescription drug bottle label for Amlodipine Besylate and Benazepril Hydrochloride capsules, clearly showing the Bryant Ranch Prepack branding in red and blue text. The label indicates oral capsules, with strengths including 5 mg and 10 mg for Amlodipine Besylate combined with 1 mg for Benazepril Hydrochloride. The label includes directions and warnings sections, and a NDC barcode at the bottom.*

FDA Label Image

Label (Lbl713352634)

Label for Amlodipine Besylate and Benazepril Hydrochloride Capsules USP, 5 mg/10 mg strength. The label includes the NDC 71335-2634-1, states the package contains 30 capsules, and shows Bryant Ranch Prepack as the repackager and Lupin Limited as the manufacturer. Storage instructions and lot/expiration details appear, with QR codes for additional information.*

* 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.