Geodon Injection, Powder, Lyophilized, For Solution
Product Images NDC 58151-137

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Geodon (NDC 58151-137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viatris Specialty Llc, 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

Structural Formula (Image 01)

Chemical structure of ziprasidone, the active ingredient in Geodon capsules, showing its molecular framework with characteristic ring systems, including a chlorinated aromatic ring and nitrogen- and sulfur-containing groups.*

FDA Label Image

Geodon 20 mg Container Label (Image 02)

Geodon (ziprasidone) 20 mg capsules packaging label showing the product name, generic name, dosage strength, and quantity of 60 capsules. The label indicates it is distributed by Viatris Specialty LLC and includes storage instructions, Rx only status, lot number, and expiration date area.*

FDA Label Image

Geodon 40 mg Container Label (Image 03)

Label for Geodon (ziprasidone) capsules, 40 mg strength, oral dosage form. The package contains 60 capsules and is labeled for prescription use only. Distributed by Viatris Specialty LLC, with storage instructions and lot/expiry details provided.*

FDA Label Image

Geodon 60 mg Container Label (Image 04)

Label for Geodon capsules containing ziprasidone 60 mg by Viatris Specialty LLC. The packaging indicates 60 capsules per container, includes storage instructions, dosage reference, and identification codes such as NDC and GTIN. The capsules are prescription only and labeled as made in Ireland.*

FDA Label Image

Geodon 80 mg Container Label (Image 05)

Geodon (ziprasidone) capsules, 80 mg strength, packaged as 60 capsules. The label includes storage instructions, dosage form as oral capsules, and is labeled by Viatris Specialty LLC. The packaging shows the NDC number 58151-134-91 and indicates prescription use only.*

FDA Label Image

Geodon 20 mg/ml Carton Label (Image 06)

Box label for Geodon for Injection, containing 10 single dose vials of ziprasidone mesylate. The strength is 20 mg/mL of ziprasidone. The label states it is sterile and for intramuscular use only, with a warning to protect from light. The product is distributed by Viatris Specialty LLC.*

* 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.