Geodon
Product Images NDC 0049-3960

19 FDA label images from Roerig · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Geodon (NDC 0049-3960). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Roerig, 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

Chemical Structure (Geodon 01)

Chemical Structure (Geodon 01)
Chemical structure diagram of the active ingredient in Geodon, showing its molecular arrangement including heterocyclic rings containing sulfur and nitrogen atoms, a chlorinated aromatic ring, and additional functional groups.*
FDA Label Image

Logo (Geodon 02)

FDA Label Image

Logo (Geodon 02a)

FDA Label Image

Principal Display Panel (20 mg Capsule Bottle Label)

Principal Display Panel (20 mg Capsule Bottle Label)
Geodon 20 mg capsules label by ROERIG under Pfizer, containing ziprasidone HCl. The label states storage instructions at 25°C with permitted excursions and notes 60 capsules in the package. It is for Rx only and made in Ireland. The NDC number is 0049-3960-60.*
FDA Label Image

Principal Display Panel (60 mg Capsule Bottle Label)

Principal Display Panel (60 mg Capsule Bottle Label)
Label for Geodon 60 mg capsules, containing the active ingredient ziprasidone hydrochloride. The label indicates 60 capsules per container, with storage instructions at 25°C (77°F) and dosage reference to accompanying prescribing information. Manufactured by Roerig and distributed by Pfizer, marked as Rx only.*
FDA Label Image

Principal Display Panel (80 mg Capsule Bottle Label)

Principal Display Panel (80 mg Capsule Bottle Label)
Geodon 80 mg capsules label by ROERIG (Pfizer). Contains ziprasidone HCl, 80 mg strength, with 60 capsules per container. The label includes storage instructions at 25°C (77°F), dosage guidance to refer to accompanying prescribing information, and states the product is made in Ireland. Marked Rx only.*
FDA Label Image

Principal Display Panel (20 mg/mL Single Dose Vial Label)

Principal Display Panel (20 mg/mL Single Dose Vial Label)
Label for Geodon for Injection (ziprasidone mesylate) sterile single dose vial. The label indicates 20 mg/mL strength equivalent of ziprasidone. It includes storage instructions, preparation details to reconstitute to 20 mg/mL with sterile water for injection, and notes for intramuscular use only. The labeler is Roerig, a division of Pfizer Inc.*
FDA Label Image

Principal Display Panel (20 mg/mL Vial Carton)

Principal Display Panel (20 mg/mL Vial Carton)
Box packaging label for Geodon for Injection sterile injectable solution, containing 20 mg/mL of ziprasidone mesylate. The label indicates it is for a single dose vial and for intramuscular use only. The manufacturer is Pfizer, distributed by Roerig, a division of Pfizer Inc. Storage instructions specify 25°C with permitted excursions and protection from light. The label also includes dosage and reconstitution directions.*
FDA Label Image

Principal Display Panel (10 Vial Carton)

Principal Display Panel (10 Vial Carton)
Geodon for Injection 20 mg/mL (ziprasidone mesylate) packaging label for 10 single-dose vials. The label displays branding with purple and black design elements and includes the Pfizer logo. It indicates the product is sterile and for intramuscular use only. The label also features dosage information and storage instructions, and is distributed by Roerig, a division of Pfizer Inc.*
FDA Label Image

Geodon 08a

Geodon 08a
The label for Geodon for Injection (ziprasidone mesylate) shows a single dose vial containing a 20 mg/mL strength of ziprasidone. It includes storage instructions at 25°C (77°F) with light protection warnings. The product is sterile, intended for intramuscular use only, and labeled as prescription-only. The labeler is ROERIG, a division of Pfizer Inc.*
FDA Label Image

Geodon 08b

Geodon 08b
Geodon for Injection 20 mg/mL (ziprasidone mesylate) vial packaging label by Roerig, a division of Pfizer Inc. The label indicates 10 single dose vials of sterile injection for intramuscular use only. It states protection from light and includes NDC codes as well as handling and storage instructions.*
FDA Label Image

Principal Display Panel (20 mg Capsule Bottle Label)

Principal Display Panel (20 mg Capsule Bottle Label)
Label for Geodon 20 mg capsules containing ziprasidone HCl. The label indicates 60 capsules per container, for prescription use only. Distributed by Roerig, a division of Pfizer Inc., made in Ireland. Storage instructions specify controlled room temperature with excursions permitted. UPC and lot/expiration barcode are also shown.*
FDA Label Image

Principal Display Panel (40 mg Capsule Bottle Label)

Principal Display Panel (40 mg Capsule Bottle Label)
Label for Geodon (ziprasidone HCl) capsules, 40 mg strength, manufactured by Roerig (Pfizer division). The label specifies a 60 capsule count, lists storage instructions at 25°C with permitted excursions, and indicates the product is Rx only. The NDC number is 0049-0054-60, and the product is made in Ireland.*
FDA Label Image

Principal Display Panel (60 mg Capsule Bottle Label)

Principal Display Panel (60 mg Capsule Bottle Label)
Label for Geodon (ziprasidone HCl) capsules, 60 mg strength, in a 60-capsule package. The label includes storage instructions, dosage information, and states it is distributed by Roerig, a division of Pfizer Inc. The product is made in Ireland and is prescription only.*
FDA Label Image

Principal Display Panel (80 mg Capsule Bottle Label)

Principal Display Panel (80 mg Capsule Bottle Label)
Geodon 80 mg capsules label showing the active ingredient ziprasidone HCl. The label includes storage instructions, dosing guidance reference, and states each capsule contains ziprasidone hydrochloride monohydrate equivalent to 80 mg ziprasidone. Packaging details note 60 capsules per container, distributed by Roerig, division of Pfizer Inc. The label also shows the product NDC 0049-0058-60 and indicates the capsules are prescription only.*
FDA Label Image

Principal Display Panel (20 mg Capsule Bottle Label)

Principal Display Panel (20 mg Capsule Bottle Label)
Geodon 20 mg capsules label showing the active ingredient ziprasidone. The label indicates 60 capsules per container, distributed by Roerig, a division of Pfizer Inc, and made in Ireland. Storage instructions and dosage use notes are included. The label displays the NDC 0049-0352-60 and Pfizer logo.*
FDA Label Image

Principal Display Panel (40 mg Capsule Bottle Label)

Principal Display Panel (40 mg Capsule Bottle Label)
Geodon 40 mg capsules label shows the Pfizer logo, NDC 0049-0354-60, and active ingredient ziprasidone. The label specifies 60 capsules per container and is distributed by Roerig, Division of Pfizer Inc. Storage instructions are provided, and the product is made in Ireland. The label includes a barcode and sections for GTIN, lot number, and expiration date.*
FDA Label Image

Principal Display Panel (60 mg Capsule Bottle Label)

Principal Display Panel (60 mg Capsule Bottle Label)
Label for Geodon (ziprasidone) capsules, 60 mg strength, produced by Roerig, a division of Pfizer Inc. The label includes storage instructions permitting excursions between 59°F to 86°F and indicates the carton contains 60 capsules. The label shows the NDC 0049-0356-60 and includes both barcode and GTIN information with lot and expiration details provided on a blacked-out section.*
FDA Label Image

Principal Display Panel (80 mg Capsule Bottle Label)

Principal Display Panel (80 mg Capsule Bottle Label)
Label for Geodon capsules, 80 mg strength, containing ziprasidone. The label indicates 60 capsules per container, with the Pfizer logo present and Roerig as the distributor. Storage instructions specify 25°C (77°F) with permitted excursions and note the capsules contain ziprasidone hydrochloride monohydrate equivalent to 80 mg ziprasidone. The label includes barcode and NDC 0049-0358-60.*

* 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.