Tacrolimus Capsule
Product Images NDC 55111-525

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tacrolimus (NDC 55111-525). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories 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

Container1 (Container1)

Tacrolimus Capsules USP 0.5 mg label from Dr. Reddy's Laboratories Limited. The label indicates a quantity of 100 capsules, for oral use, prescription only. It includes dosage and storage information, a barcode, QR code for patient information, and the manufacturer details.*

FDA Label Image

Container2 (Container2)

Tacrolimus Capsules, USP 1 mg oral capsules label by Dr. Reddy's Laboratories Limited. The label indicates a package quantity of 100 capsules, with directions for dispensing a Patient Information Sheet. It includes the NDC 55111-526-01, barcode, QR code for patient information, and manufacturer address in Bachupally, India.*

FDA Label Image

Container3 (Container3)

Packaging label for Tacrolimus Capsules USP 5 mg by Dr. Reddy's Laboratories Limited. The label includes the NDC number 55111-527-01 and indicates prescription-only status for 100 capsules. It also features directions for patient information access, storage instructions, a barcode, and the manufacturer details with an address in India.*

FDA Label Image

Structure (Structure)

Chemical structure of the active ingredient Tacrolimus, showing its detailed molecular arrangement including hydroxyl, methoxy, and carbonyl functional groups, as well as water of hydration (H2O).*

* 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.