Calcitriol Capsule, Liquid Filled
Product Images NDC 62756-967

3 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Calcitriol (NDC 62756-967). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

0-25mcglabel (0 25mcglabel)

0-25mcglabel (0 25mcglabel)
Label for Calcitriol Capsules 0.25 mcg oral liquid-filled capsules by Sun Pharmaceutical Industries, Inc. The label indicates a quantity of 100 capsules, child-resistant packaging, and storage instructions at 20° to 25°C with light protection. The label includes the NDC code 62756-967-88 and manufacturing information from Sun Pharmaceutical Industries Ltd., Gujarat, India.*
FDA Label Image

0-5mcglabel (0 5mcglabel)

0-5mcglabel (0 5mcglabel)
Label for Calcitriol Capsules 0.5 mcg liquid filled capsules, manufactured by Sun Pharmaceutical Industries, Inc. The label states the package contains 100 capsules and indicates child-resistant packaging. Storage instructions specify 20° to 25°C with allowed excursions and protection from light. The label includes the NDC barcode and distributor and manufacturer information located in New Jersey, USA, and Gujarat, India respectively.*
FDA Label Image

Chemical-structure (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure of Calcitriol, showing its molecular arrangement with labeled carbon positions and hydroxyl groups.*

* 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.