Ziprasidone Hydrochloride
Product Images NDC 64725-2164

3 FDA label images from Tya Pharmaceuticals · 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 64725-2164). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya Pharmaceuticals, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structural Formula (0d763aa4 Bc18 430a Baa1 266b6849d534 01)

Structural Formula (0d763aa4 Bc18 430a Baa1 266b6849d534 01)
Chemical structure of ziprasidone hydrochloride showing its molecular framework with characteristic rings and bonds.*
FDA Label Image

Label Image (64725 2164)

Label Image (64725 2164)
A black and white packaging label for ziprasidone hydrochloride 20 mg capsules, showing a quantity of 30 capsules. The label indicates prescription use only, listing the manufacturer as Sandoz and repackager as T.Y.A. Pharmaceuticals, located in Tallahassee, Florida. A barcode is present along with placeholders for lot number and expiration date. Instructions note to see the package insert for dosing.*
FDA Label Image

Label Image (64725 2168)

Label Image (64725 2168)
A label for ziprasidone hydrochloride 80 mg capsules in a 30 count container. The label states the medication is prescription only and manufactured by Sandoz. It is repackaged by TYA Pharmaceuticals with address and contact information. The label includes placeholders for lot number and expiration date, a barcode, and a note to see the package insert for dosing information.*

* 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.