Ziprasidone Capsule
Product Images NDC 70518-4711

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ziprasidone (NDC 70518-4711). 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

Remedy_label (Remedy Label)

Ziprasidone Capsule 40 mg oral dosage form, packaged as a single capsule. Label shows the NDC 70518-4711-01, repackaged by RemedyRepack Inc. in Indiana. Capsule color is indicated as purple/blue. Additional storage instructions and manufacturer details for Dr. Reddy's Labs are partially visible.*

FDA Label Image

Mm1 (Ziprasidone 40mg 70518 4711 00)

Label for ziprasidone 40 mg oral capsules, repackaged by RemedyRepack Inc. The label indicates a quantity of 50 capsules per box, with capsules described as purple/blue. It includes storage instructions and a QR code, and lists the original manufacturer as Dr. Reddy's Labs.*

FDA Label Image

Mm3 (Ziprasidone 40mg 70518 4711 02)

ziprasidone 40 mg oral capsules packaging label showing a quantity of 30 capsules. The label includes the NDC number 70518-4711-02 and indicates the capsules are purple and blue. It is repackaged by RemedyRepack Inc., located in Indiana, PA. Additional storage instructions and manufacturer information for Dr. Reddy's Labs, Princeton, NJ, are also noted.*

FDA Label Image

Structure (Structure)

Chemical structure of ziprasidone shown as a skeletal formula with rings, nitrogen, sulfur, chlorine atoms, and a ketone group, representing the molecular arrangement of the active ingredient.*

* 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.