Amlodipine And Benazepril Hydrochloride Capsule
Product Images NDC 57237-146

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 57237-146). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

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

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, 2.5 mg/10 mg strength, packaged with 100 capsules. The label includes storage instructions, distributor information (Rising Health, LLC), and a barcode. It is marked for prescription use only and notes the product is made in India.*

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 by Rising Pharma Holdings, Inc. The label indicates a quantity of 100 capsules, prescription only, and includes dosage information specifying the active ingredients' amounts per capsule. Storage instructions specify temperature ranges and moisture protection. Distributed by Rising Health, LLC, with manufacturing in India. Barcode and revision date 12/2021 are visible.*

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, showing a 100-capsule package. The label includes the NDC 57237-144-01, storage instructions, distributor information for Rising Health, LLC, Saddle Brook, NJ, and a barcode. The product is marked Rx only and made in India.*

FDA Label Image

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

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, strength 5 mg/40 mg, in a 100 capsule package. The label shows the Rising brand logo and indicates the product is Rx only. It includes storage instructions, dosage caution to see prescribing information, and distributor details for Rising Health, LLC. The capsules are made in India.*

FDA Label Image

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

Label for Amlodipine and Benazepril Hydrochloride Capsules USP, strength 10 mg/20 mg. The label states a quantity of 100 capsules, for oral use, prescription only. It is produced by Rising Pharma Holdings, Inc. and distributed by Rising Health, LLC. The label includes storage instructions, ingredients, and manufacturing details with an emphasis on protecting from moisture.*

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, in a container of 100 capsules. The label shows dosage strength, manufacturer Rising Pharma Holdings, and distributor Rising Health, LLC. It includes storage instructions, a barcode, and prescription-only designation.*

FDA Label Image

Amlodipine Besylate Chemical Structure (Amlobenaz Str1)

Chemical structure of Amlodipine and Benazepril Hydrochloride showing molecular components, including aromatic rings and various functional groups, along with an HCl moiety.*

FDA Label Image

Benazepril Hydrochloride Chemical Structure (Amlobenaz Str2)

Chemical structure diagram showing molecular representations for Amlodipine and Benazepril Hydrochloride, the active ingredients in the product. The diagram illustrates the arrangement of various functional groups and atoms typical for these compounds without specific atomic detail.*

* 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.