Cyclosporine Capsule, Liquid Filled
Product Images NDC 23155-837

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Cyclosporine (NDC 23155-837). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals 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

Chemical Structure (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 01)

Chemical structure diagram of cyclosporine, showing its molecular formula C62H111N11O12 and molecular weight 1202.63. The structure includes various amino acid residues represented by abbreviations such as MeVal, MeLeu, D-Ala, Ala, Abu, and MeGly.*

FDA Label Image

Graph (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 02)

A bar chart titled 'ACR Responders Randomized' compares response rates among various treatment groups, including Cyclosporine (CsA), Methotrexate (Mtx), placebo (pla), their combinations, and Cyclosporine capsules USP (modified). The chart shows percentages on the y-axis (0% to 50%) and lists sample sizes and p-values above the bars, indicating statistical comparisons vs. placebo or between treatments.*

FDA Label Image

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FDA Label Image

Image (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 04)

Packaging label for Cyclosporine Capsules USP (Modified) 25 mg soft gelatin capsules by Heritage Pharmaceuticals Inc. The label indicates 30 soft gelatin capsules per package for oral use with dosage and storage instructions. The label includes barcode, manufacturer details, and removal instructions for the capsules.*

FDA Label Image

Image (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 05)

Label sheet showing multiple identical labels for Cyclosporine Capsule, USP (Modified) 25 mg. Each label includes the proprietary name Cyclosporine, dosage form as capsule, 25 mg strength, and is manufactured by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The labels also display the NDC 23155-837-11, barcode, and storage instructions. Labels are arranged in a grid layout on a 185 mm tall sheet.*

FDA Label Image

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Packaging label for cyclosporine capsules, USP (modified) in 50 mg soft gelatin capsules form. The label shows a 30-count bottle package by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label includes usage and safety instructions along with barcodes and manufacturer details.*

FDA Label Image

Image (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 07)

Packaging label for CYCLOSPORINE 50 mg capsules, liquid-filled, oral use. The labels specify the active ingredient cyclosporine with 50 mg strength. The labels indicate the product contains dehydrated alcohol and is produced by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. Barcode, lot number, and expiration date fields are visible but not fully legible.*

FDA Label Image

Image (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 08)

Packaging label for cycloSPORINE Capsules USP (MODIFIED) 100 mg, soft gelatin capsules. The label indicates a 30-capsule count, oral route, and is marked as prescription only. The labeler is Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label includes dosage and storage information, and child-resistant closure directions with pictograms.*

FDA Label Image

Image (167e1a72 631a 4d4a 81ff 3cc435cd7ba5 09)

Label sheet for Cyclosporine Capsule, USP (Modified) 100 mg, liquid filled oral capsules. Each label includes the product name, strength, NDC code 23155-839-11, and manufacturer information showing Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., East Brunswick, NJ. Labels note the content of dehydrated alcohol and include placeholder fields for lot number and expiration date. The sheet contains multiple identical labels arranged in a grid format.*

* 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.