Amlodipine Besylate And Benazepril Hydrochloride
Product Images NDC 58118-2272

Product Visual Gallery

This gallery contains 26 technical images submitted to the FDA as part of the official labeling for Amlodipine Besylate And Benazepril Hydrochloride (NDC 58118-2272). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, 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 – 10 mg/ 20 mg (Amlben10.20lab00)

Packaging label for Amlodipine Besylate and Benazepril Hydrochloride, showing strength of 10-20 mg. The label indicates the drug form as capsules, manufactured by Sandoz, and distributed by Clinical Solutions Wholesale. It includes a barcode, lot, and expiration date fields, plus contact phone number for Clinical Solutions.*

FDA Label Image

10 mg/ 20 mg (Amlben10.20lab08)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, 10-20 mg strength in capsule form. The package contains 30 capsules. Labeler is Clinical Solutions Wholesale. Includes NDC 58118-2274-8 and manufacturer Sandoz Inc., with manufacturer NDC 0781-2274-01. Additional label details include lot number, expiration, and a QR code.*

FDA Label Image

10 mg/ 20 mg (Amlben10.20lab09)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, 10-20 mg, packaged as 90 capsules. The label includes the NDC 58118-2274-9, barcode, dosing strength, quantity, lot number, fill date, expiration date, and manufacturer information (Sandoz Inc.). Labeled by Clinical Solutions Wholesale.*

FDA Label Image

10 mg/ 20 mg (Amlben10.20lab30)

A prescription label for Amlodipine Besylate and Benazepril HCL Tablets, USP, with strengths of 10-20 mg. The label indicates a bottle containing 30 capsules, distributed by Clinical Solutions Wholesale and manufactured by Sandoz Inc. It includes NDC numbers, lot number, expiration date, and a QR code.*

FDA Label Image

Package Label – 10 mg/ 40 mg (Amlben10.40lab00)

Label for Amlodipine Besylate and Benazepril Hydrochloride showing a quantity of 1 with dosage 10-40 mg. The label mentions blue/cap Lotrel 0379, manufactured by Sandoz, includes a barcode, and contact information for Clinical Solutions Wholesale pharmacy. The bag count is 1 and fields for lot and expiration date are present but blank.*

FDA Label Image

10 mg/ 40 mg (Amlben10.40lab08)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, with strengths ranging from 10 to 40 mg. The bottle contains 30 capsules. The label shows the NDC number 58118-2279-8 and indicates distribution by Clinical Solutions Wholesale. Manufacturer is Sandoz Inc. The label includes fill and expiration dates, a barcode, and a QR code.*

FDA Label Image

10 mg/ 40 mg (Amlben10.40lab09)

Packaging label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, with a strength range of 10-40 mg. The label indicates 90 capsules per package, distributed by Clinical Solutions Wholesale. Additional details include an NDC, lot number, expiration date, and manufacturer information citing Sandoz Inc.*

FDA Label Image

10 mg/ 40 mg (Amlben10.40lab30)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, strength 10-40 MG, containing 30 capsules. The label shows the product name, dosage form, count, and manufacturer as Sandoz Inc. Distributed by Clinical Solutions Wholesale. Includes NDC numbers, lot number, fill and expiration dates, and storage instructions.*

FDA Label Image

Package Label – 2.5 mg/ 10 mg (Amlben2.5.10lab00)

Label for Amlodipine Besylate and Benazepril Hydrochloride showing dosage strengths 2.5-10 mg. Container color is white and yellow with a cap labeled Sandoz 571. Manufactured by Sandoz. Includes lot number, barcode, and an empty field for expiration date. Labeler is Clinical Solutions Wholesale with a phone number provided. Package indicated as Bag 1.*

FDA Label Image

2.5 mg/ 10 mg (Amlben2.5.10lab08)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP 2.5-10MG, packaged as 30 capsules by Clinical Solutions Wholesale. The label includes NDC 58118-2271-8, lot number 123lotnum, fill date 03/13/13, expiration 03/15/15, and manufacturer Sandoz Inc. A barcode and QR code are also present.*

FDA Label Image

2.5 mg/ 10 mg (Amlben2.5.10lab09)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, 2.5-10 mg strength, containing 90 capsules. Distributed by Clinical Solutions Wholesale, includes NDC 58118-2271-9 and manufacturer information for Sandoz Inc. Barcode and QR code present.*

FDA Label Image

2.5 mg/ 10 mg (Amlben2.5.10lab30)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, strength 2.5-10 mg, containing 30 capsules. Distributed by Clinical Solutions Wholesale and manufactured by Sandoz Inc. Includes NDC 58118-2271-3, lot number, fill and expiration dates, and a QR code. Label indicates prescription-only status.*

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Package Label – 5 mg/ 10 mg (Amlben5.10lab00)

Label for Amlodipine Besylate and Benazepril Hydrochloride showing strengths 5-10mg. It indicates packaging as yellow capsule style Sandoz 572, manufacturer Sandoz, with barcode and lot/expiration date placeholders. Labeler is Clinical Solutions Wholesale with phone contact 877-826-5488. Quantity stated as 1 bag.*

FDA Label Image

5 mg/ 10 mg (Amlben5.10lab08)

Packaging label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, 5-10 mg strength, containing 30 capsules. The label shows the Clinical Solutions Wholesale labeler, includes an NDC number 58118-2272-8, lot number 123lotnum, fill date 03/13/13, and expiration date 03/15/15. Manufacturer is Sandoz Inc. The label features a barcode and a QR code.*

FDA Label Image

5 mg/ 10 mg (Amlben5.10lab09)

Packaging label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, in 5-10 mg strength. The label shows a quantity of 90 capsules, RX only, distributed by Clinical Solutions Wholesale, with manufacturer Sandoz Inc. Lot, fill, and expiration dates are present, along with barcodes and a QR code.*

FDA Label Image

5 mg/ 10 mg (Amlben5.10lab30)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, 5-10MG strength, packaged as 30 capsules. Distributed by Clinical Solutions Wholesale with NDC 58118-2272-3. Includes lot number, expiration date, barcode, and manufacturer details (Sandoz Inc.).*

FDA Label Image

Package Label – 5 mg/ 20 mg (Amlben5.20lab00)

Label for Amlodipine Besylate and Benazepril Hydrochloride 5-20mg capsules. It includes the product quantity (Q: 1), description indicating pink capsules from Sandoz, manufacturer Sandoz, and a barcode with the number 58118-2273-0. The label also lists Clinical Solutions Wholesale as the labeler with a contact phone number and a bag count of 1.*

FDA Label Image

5 mg/ 20 mg (Amlben5.20lab08)

Label for Amlodipine Besylate and Benazepril Hydrochloride USP Tablets 5-20 mg, containing 30 capsules. The product is labeled Rx only and distributed by Clinical Solutions Wholesale. The label includes lot number, expiration date, manufacturer information, barcode, and a QR code.*

FDA Label Image

5 mg/ 20 mg (Amlben5.20lab09)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, 5-20 mg, in a package containing 90 capsules. The label shows the labeler as Clinical Solutions Wholesale with NDC 58118-2273-9 and manufacturer Sandoz Inc. It includes a fill date of 03/13/13 and an expiration date of 03/15/15. Storage instructions and lot number details are also visible.*

FDA Label Image

5 mg/ 20 mg (Amlben5.20lab30)

Label for Amlodipine Besylate and Benazepril Hydrochloride (HCL) Tablets USP, strength 5-20 MG, in a package containing 30 capsules. Distributed by Clinical Solutions Wholesale, includes barcode, NDC 58118-2273-3, lot number 123lotnum, manufacture and expiration dates, and manufacturer Sandoz Inc. A QR code appears on the label.*

FDA Label Image

Package Label – 5 mg/ 40 mg (Amlben5.40lab00)

Label for Amlodipine Besylate and Benazepril Hydrochloride showing a quantity of 1 tablet with strength range 5-40 mg. The label notes a blue description and cap, manufacturer Sandoz, along with a barcode, lot information, expiration date placeholder, and contact phone number for Clinical Solutions Wholesale. The bag count is 1.*

FDA Label Image

5 mg/ 40 mg (Amlben5.40lab08)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, 5-40 mg strength, containing 30 capsules. The product is labeled by Clinical Solutions Wholesale and manufactured by Sandoz Inc. The label includes the NDC 58118-2277-8, lot number, fill date, and expiration date.*

FDA Label Image

5 mg/ 40 mg (Amlben5.40lab09)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets USP, 5-40 mg, distributed by Clinical Solutions Wholesale. The package contains 90 capsules. The label includes the NDC number 58118-2277-9, lot number 123lotnum, and expiration date 03/15/15. Manufacturer is Sandoz Inc. The label also features a QR code and storage instructions.*

FDA Label Image

5 mg/ 40 mg (Amlben5.40lab30)

Label for Amlodipine Besylate and Benazepril Hydrochloride Tablets, USP, 5-40MG strength, containing 30 capsules. The product is distributed by Clinical Solutions Wholesale and manufactured by Sandoz Inc. The label includes NDC 58118-2277-3 and batch information such as lot number and expiration date.*

FDA Label Image

Benazepril Hydrochloride Structural Formula (Amlbenchemstruc1)

Chemical structure of benazepril hydrochloride, showing its molecular arrangement including carbon, hydrogen, nitrogen, and oxygen atoms.*

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Amlodipine Besylate Structural Formula (Amlbenchemstruc2)

Chemical structure of Amlodipine Besylate and Benazepril Hydrochloride, showing molecular components including phenyl rings, chlorine, methoxy groups, and sulfonic acid moieties as typically found in the active ingredients' chemical representation.*

* 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.