Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 65862-583

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Amlodipine And Benazepril Hydrochloride (NDC 65862-583). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (2.5 mg/10 mg (100 Capsules Bottle))

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, strength 2.5 mg/10 mg. The label indicates the product is Rx only, distributed by Aurobindo Pharma USA, Inc., with a package count of 100 capsules. It includes storage instructions, recommended dosage reference, and a barcode on the right side.*

FDA Label Image

Package Label-principal Display Panel (5 mg/10 mg (100 Capsules Bottle))

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, 5 mg/10 mg strength, manufactured by Aurobindo Pharma Limited. The label indicates the product is for prescription use only, contains 100 capsules, and details storage instructions along with the distributor's information, Aurobindo Pharma USA, Inc. The label includes a barcode and dosage information emphasizing prescription reference.*

FDA Label Image

Package Label-principal Display Panel (5 mg/20 mg (100 Capsules Bottle))

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, 5 mg/20 mg strength. The label indicates it is for Rx only and contains 100 capsules. Distributed by Aurobindo Pharma USA, Inc., made in India. Storage instructions and dosage references are included, along with a barcode and overprint zone marking.*

FDA Label Image

Package Label-principal Display Panel (5 mg/40 mg (100 Capsules Bottle))

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, 5 mg/40 mg strength, containing 100 capsules. Distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions, recommended dosage note, and a barcode. It also shows the labeler as Aurobindo Pharma Limited, with emphasis on 'Rx only' prescription status.*

FDA Label Image

Package Label-principal Display Panel (10 mg/20 mg (100 Capsules Bottle))

Packaging label for Amlodipine and Benazepril Hydrochloride Capsules USP 10 mg/20 mg by Aurobindo Pharma Limited. The label includes dosage strength, quantity of 100 capsules, storage instructions, and distributor information from Aurobindo Pharma USA. The label emphasizes prescription use and lists a yellow color additive.*

FDA Label Image

Package Label-principal Display Panel (10 mg/40 mg (100 Capsules Bottle))

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, 10 mg/40 mg strength, containing 100 capsules. The label shows the NDC 65862-587-01, identifies the product as Rx only, and lists Aurobindo Pharma Limited as the labeler. Additional information includes storage conditions, recommended dosage reference, and origin (Made in India). Aurobindo Pharma USA address is also provided.*

FDA Label Image

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)

Chemical structure diagram of Amlodipine and Benazepril Hydrochloride, depicting molecular bonds and atom connectivity including a benzene ring and hydrochloride ion.*

FDA Label Image

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)

Chemical structure diagram showing molecular formulas of two compounds. The structures include rings and functional groups, consistent with active ingredients in pharmaceuticals, likely representing Amlodipine and Benazepril Hydrochloride.*

* 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.