Amlodipine Besylate And Benazepril Hydrochloride Capsule
Product Images NDC 68001-133

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate And Benazepril Hydrochloride (NDC 68001-133). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Amlo (97c31cbc Cd3b 4029 92eb 6215cdaa6e66 01)

Amlo (97c31cbc Cd3b 4029 92eb 6215cdaa6e66 01)
Chemical structure diagram of Amlodipine Besylate, showing its molecular components including benzene rings, chloride (Cl) group, ester groups, and sulfonic acid (SO3H) group. This structural formula represents the active ingredient in the Amlodipine Besylate and Benazepril Hydrochloride drug product.*
FDA Label Image

Benza (97c31cbc Cd3b 4029 92eb 6215cdaa6e66 02)

Benza (97c31cbc Cd3b 4029 92eb 6215cdaa6e66 02)
Chemical structure of the active ingredient Benazepril Hydrochloride, showing its molecular arrangement including a phenyl ring, lactam ring, and hydrochloride salt component.*
FDA Label Image

Image 01

Image 01
Label for Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg by BluePoint Laboratories. The label indicates prescription use only, with 100 capsules in the container. It includes storage instructions, manufacturer details (Lupin Limited, India), and a barcode. Dosage and protection information is also shown.*
FDA Label Image

Image 02

Image 02
Amlodipine Besylate and Benazepril HCl Capsules USP label showing 5 mg/10 mg strength. The label includes dosage information, storage instructions, manufacturer details (Lupin Limited, Goa, India), and package size of 100 capsules. It displays the NDC 68001-133-00 and BluePoint Laboratories as the labeler.*
FDA Label Image

Image 03

Image 03
Label for Amlodipine and Benazepril HCl Capsules USP 5 mg/20 mg by BluePoint Laboratories. The label shows the active ingredient amounts per capsule, storage instructions, manufacturer Lupin Limited in Goa, India, and package size of 100 capsules. The NDC code is 68001-134-00.*
FDA Label Image

Image 04

Image 04
Label for Amlodipine and Benazepril HCl Capsules USP 5mg/40mg by BluePoint Laboratories. The label states 100 capsules per container and includes dosage and storage instructions, manufacturer details (Lupin Limited, Goa, India), and a barcode. It notes the product is Rx Only and includes the NDC 68001-135-00.*
FDA Label Image

Image 05

Image 05
Packaging label for Amlodipine and Benazepril HCl Capsules USP, 10 mg/20 mg strength. The label shows a white and red design with dosage information, manufacturer Lupin Limited in India, and a 100 capsule package. It includes storage and handling instructions, barcode, and BluePoint Laboratories branding.*
FDA Label Image

Image 06

Image 06
Label for Amlodipine Besylate and Benazepril Hydrochloride Capsules USP, containing 10 mg/40 mg strength. The label states it is a prescription drug with 100 capsules per container, manufactured by BluePoint Laboratories. Storage and dosage information are included, along with a barcode and manufacturer details from Lupin Limited, Goa, India.*
FDA Label Image

Amlo Ben HCl Label 2.5mg10mg Rev 12-16 (Image 07)

Amlo Ben HCl Label 2.5mg10mg Rev 12-16 (Image 07)
Label for Amlodipine Besylate and Benazepril Hydrochloride Capsules USP 2.5 mg/10 mg, oral capsules, prescription drug by BluePoint Laboratories. The label includes dosage strengths, storage instructions, manufacturer (Lupin Limited, India), and a barcode. The package contains 100 capsules.*
FDA Label Image

Amlo Ben HCl Label 5mg10mg Rev 12-16 (Image 08)

Amlo Ben HCl Label 5mg10mg Rev 12-16 (Image 08)
Label for Amlodipine Besylate and Benazepril Hydrochloride Capsules USP, 5 mg/10 mg, by BluePoint Laboratories. The label includes dosage form as capsules, prescription only status, NDC 68001-133-00, and a quantity of 100 capsules. It provides storage instructions and manufacturer information for Lupin Limited, India.*
FDA Label Image

Amlo Ben HCl Label 5mg20mg Rev 12-16 (Image 09)

Amlo Ben HCl Label 5mg20mg Rev 12-16 (Image 09)
Label for Amlodipine and Benazepril HCl Capsules USP, 5 mg/20 mg strength, in a 100-capsule package by BluePoint Laboratories. The label includes dosing instructions, storage conditions, manufacturer Lupin Limited in India, NDC 68001-134-00, and a barcode. It states the product is Rx only and provides warnings about moisture protection and keeping medication away from children.*
FDA Label Image

Amlo Ben HCl Label 5mg40mg Rev 12-16 (Image 10)

Amlo Ben HCl Label 5mg40mg Rev 12-16 (Image 10)
Label for Amlodipine and Benazepril HCl Capsules USP, 5 mg/40 mg strength. The label shows the drug name, dosage form as capsules, prescription status (Rx Only), and package size of 100 capsules. It includes storage instructions at 25°C and manufacturer details for BluePoint Laboratories and Lupin Limited, India. A barcode and NDC 68001-135-00 are visible.*
FDA Label Image

Amlo Ben HCl Label 10mg20mg Rev 12-16 (Image 11)

Amlo Ben HCl Label 10mg20mg Rev 12-16 (Image 11)
Packaging label for Amlodipine and Benazepril HCl Capsules USP 10 mg/20 mg by BluePoint Laboratories. The label includes dosage details, storage instructions, manufacturer Lupin Limited in India, and package size of 100 capsules. The label features drug listing, NDC 68001-130-00, and a barcode.*
FDA Label Image

Amlo Ben HCl Label 10mg40mg Rev 12-16 (Image 12)

Amlo Ben HCl Label 10mg40mg Rev 12-16 (Image 12)
Label for Amlodipine Besylate and Benazepril Hydrochloride Capsules USP, 10 mg/40 mg strength, from BluePoint Laboratories. The label indicates a package containing 100 capsules. It includes dosage details, storage instructions, manufacturer information (Lupin Limited, India), and states the product is for prescription use only with NDC 68001-131-00.*

* 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.