Cyclosporine Capsule, Liquid Filled
Product Images NDC 64380-128

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Cyclosporine (NDC 64380-128). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science 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

Image (B82f9dde 0d55 4ffe 9662 2c88da347f57 01)

Chemical structure diagram showing a complex organic molecule with multiple amino acid residues including MeVal, MeLeu, D-Ala, Ala, MeLeu, Val, Abu, and MeGly. The formula C62H111N11O12 and molecular weight 1202.63 are indicated at the bottom.*

FDA Label Image

Image (B82f9dde 0d55 4ffe 9662 2c88da347f57 02)

A bar chart titled 'ACR Responders Randomized' comparing response rates across different treatment groups: CsA, Mtx, placebo, CsA+Mtx, placebo+Mtx, and Cyclosporine capsules USP (modified). The vertical axis shows percentage response rates from 0% to 50%, with statistical p-values noted above each comparison indicating significance relative to placebo or between treatments.*

FDA Label Image

25mg Carton (B82f9dde 0d55 4ffe 9662 2c88da347f57 03)

Packaging label for cycloSPORINE Capsules, USP (MODIFIED) 25 mg soft gelatin capsules in a package of 30 capsules. The label includes dosage strength, administration warnings, inactive ingredients, manufacturer information (Strides Pharma Inc.), and instructions for capsule removal. The label also shows barcodes and storage conditions, indicating it is an Rx-only medication.*

FDA Label Image

25mg Foil (B82f9dde 0d55 4ffe 9662 2c88da347f57 04)

Labels for cycloSPORINE Capsule, USP (MODIFIED) 25 mg. Each label includes the NDC 64380-127-01, barcode, and mentions the presence of dehydrated alcohol (9.5% w/v/12.0% v/v). Distributed by Strides Pharma Inc., East Brunswick, NJ 08816. Lot and expiration information are placeholders (LOT: xxxxxxxx EXP: xx/xxxx). The sheet contains multiple identical labels arranged in four columns.*

FDA Label Image

50mg Carton (B82f9dde 0d55 4ffe 9662 2c88da347f57 05)

Packaging label for cycloSPORINE Capsules, USP (MODIFIED) 50 mg, soft gelatin capsules. The carton contains 30 capsules and is labeled Rx only. Manufacturer is Strides Pharma Inc. The label includes a warning that these capsules are not bioequivalent to Sandimmune capsules and should not be interchanged without physician supervision. Additional instructions and ingredient information are displayed on the label.*

FDA Label Image

50mg-foil (B82f9dde 0d55 4ffe 9662 2c88da347f57 06)

Label sheet featuring multiple identical labels for cycloSPORINE Capsule, USP (MODIFIED), 50 mg. Each label includes the NDC code 64380-128-01, a barcode, and text indicating the presence of dehydrated alcohol (9.5% w/v/12.0% v/v). Labels state distribution by Strides Pharma Inc., East Brunswick, NJ 08816, and show placeholders for lot number and expiration date.*

FDA Label Image

100mg-carton (B82f9dde 0d55 4ffe 9662 2c88da347f57 07)

Packaging label for cyclosporine capsules USP (modified soft gelatin capsules) in a 100 mg strength. The label indicates 30 soft gelatin capsules per package. The manufacturer is Strides Pharma Inc. It includes dosage form, strength, NDC number 64380-129-02, storage instructions, inactive ingredients, warnings, and instructions for removing capsules from blister packaging.*

FDA Label Image

100mg-foil (B82f9dde 0d55 4ffe 9662 2c88da347f57 08)

This image shows multiple product labels for cycloSPORINE Capsule, USP (MODIFIED) 100 mg. Each label includes the NDC number 64380-129-01, a barcode, and mentions dehydrated alcohol (9.5% w/v/12.0% v/v). The distributor is Strides Pharma Inc., East Brunswick, NJ 08816. Lot and expiration date fields are present but not filled.*

* 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.