Ziprasidone Hydrochloride
Product Images NDC 70518-1604

View Photos of 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 Ziprasidone Hydrochloride (NDC 70518-1604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm1 (Remedy Label)

Mm1 (Remedy Label)
Label for Ziprasidone 80 mg capsules, quantity 30, repackaged by RemedyRepack Inc. The label includes the NDC 70518-1604-00, source NDC 55111-0259-60, and manufacturer Dr. Reddy's Labs, Princeton, NJ. It also includes storage instructions and a notice to keep medication out of children's reach.*
FDA Label Image

Ziprasidone 80mg 70518 1604 01

Ziprasidone 80mg 70518 1604 01
Label for Ziprasidone 80 mg capsules, repackaged by RemedyRepack Inc. The package contains 30 capsules. It includes NDC 70518-1604-01 and notes manufacturing by Dr. Reddy's Labs in Princeton, NJ. Directions advise storage at 20-25°C with permitted excursions to 15-30°C and refer to the package insert for use instructions.*
FDA Label Image

Ziprasidone 80mg 70518 1604 02

Ziprasidone 80mg 70518 1604 02
Label for ziprasidone 80 mg capsule, showing a quantity of 1. The label includes the NDC number 70518-1604-02 and states it is repackaged by RemedyRepack Inc., Indiana, PA. Manufacturer is Dr. Reddy's Labs, Princeton, NJ. Storage instructions and directions for use reference the package insert. The label includes a QR code and a warning to keep medication out of reach of children.*

* 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.