Ziprasidone Hydrochloride Capsule
Product Images NDC 70518-0787

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ziprasidone Hydrochloride (NDC 70518-0787). 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)

Label for Ziprasidone Hydrochloride 40 mg capsules, quantity of 30, repackaged by RemedyRepack Inc. The label includes the product name, strength, dosage form, and repackager information. Manufacturer is Macleods Pharma USA, Plainsboro, NJ. The label also shows the NDC number 70518-0787-00, a barcode, and a QR code, with instructions to see the package insert for directions.*

FDA Label Image

Ziprasidone 40mg 70518 0787 01

Ziprasidone Hydrochloride 40 mg capsule label indicating a quantity of 30 capsules. The label includes the NDC number 70518-0787-01 and states the manufacturer as Macleods Pharma USA, Plainsboro, NJ. It contains storage instructions and repackaging details by RemedyRepack Inc., Indiana, PA.*

FDA Label Image

Ziprasidone 40mg 70518 0787 02

Label for Ziprasidone Hydrochloride 40 mg oral capsule, quantity of 1, repackaged by RemedyRepack Inc. Includes NDC 70518-0787-02, manufacturer Macleods Pharma USA, and storage instructions. Barcode and QR code present on label.*

FDA Label Image

Str (Ziprasidone Str)

Chemical structure of Ziprasidone Hydrochloride shown as a two-dimensional molecular diagram, illustrating the arrangement of rings, nitrogen, sulfur, chlorine, and oxygen atoms in the molecule.*

* 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.