Duloxetine Capsule, Delayed Release
Product Images NDC 65841-799

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Duloxetine (NDC 65841-799). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences 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

Duloxetine Delayed-release Capsules (3006bed7 89e5 45fa B105 E6ebac56d98c 09)

Label for Duloxetine Delayed-Release Capsules USP 20 mg by Zydus Lifesciences Limited, marketed under ZyGenerics. The label states the product contains 90 capsules, is Rx only, and each capsule contains 22.4 mg duloxetine hydrochloride USP equivalent to 20 mg duloxetine. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India. Storage and dispensing instructions are also included.*

FDA Label Image

Duloxetine Delayed-release Capsules (3006bed7 89e5 45fa B105 E6ebac56d98c 10)

Duloxetine delayed-release capsules, 30 mg strength, oral dosage form, packaged by Zydus Lifesciences Limited under the ZyGenerics brand. The label states the product contains 90 capsules and includes storage instructions, manufacturer information as Cadila Healthcare Ltd., Ahmedabad, India, and safety warnings.*

FDA Label Image

Duloxetine Delayed-release Capsules (3006bed7 89e5 45fa B105 E6ebac56d98c 11)

Label for Duloxetine Delayed-Release Capsules, USP 60 mg, supplied in a bottle containing 90 capsules. The label includes dosage strength, a partial capsule image, prescription-only status, and storage instructions. Manufactured by Cadila Healthcare Ltd., Ahmedabad, India, with a note for pharmacists to dispense the medication guide separately.*

* 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.