Geodon Capsule
Product Images NDC 0049-0352
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Product Visual Gallery
This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Geodon (NDC 0049-0352). 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.
Product Images & Figures Index
Logo (Geodon 02)
Logo (Geodon 02a)
Principal Display Panel (20 mg Capsule Bottle Label)
Principal Display Panel (60 mg Capsule Bottle Label)
Geodon (ziprasidone HCI) capsules should be stored at 25°C (77°F) and can be excursed between 15-30°C (59-86°F) [see USP Controlled Room Temperature]. Each capsule contains ziprasidone hydrochloride monohydrate equivalent to 60 mg ziprasidone. More information can be found in the accompanying prescribing information. This medication is produced and distributed by Pfizer, and each pack comes with 60 capsules with NDC 0049-3980-60. This drug is indicated for the treatment of schizophrenia and bipolar disorder. Rx only. Made in Ireland.*
Principal Display Panel (80 mg Capsule Bottle Label)
This is a prescription drug called Geodon. The recommended storage temperature is 25°C (77°F), but it can be stored between 15-30°C (69-86°F). Each capsule contains 80 mg of Ziprasidone hydrochloride monohydrate equivalent to 1080 mg of ziprasidone. The drug comes in a bottle of 60 capsules and can only be obtained with a prescription. Additional information on dosage and use can be obtained from the accompanying prescribing information. The drug was manufactured in Ireland.*
Principal Display Panel (20 mg/mL Single Dose Vial Label)
Store this medicine at a temperature of 25°C (77°F), and short term variations between 15°C and 30°C (59°F to 86°F) are allowed. The medication is a single dose vial with NDC 0049-3920-20, named Geodon. It is intended for intramuscular use only, and Roerig Sterile Division of Pfizer Inc. from NY, NY 10017 distributes it. To prepare it for use, shake it until the entire drug dissolves. When reconstituted, each mL of Geodon contains 20mg of ziprasidone and 4.7 mg of methanesulfonic acid solubilized by 294mg of SBECD.*
Principal Display Panel (20 mg/mL Vial Carton)
This text is a product description for a single-dose vial of Geodon® injection medication. It contains instructions on dosage and use, as well as how to properly store the medication. The medication is intended for intramuscular use only and should be protected from light. The vial should be reconstituted with sterile water before use and can be stored at room temperature for up to 24 hours. This medication is manufactured and distributed by Roerig, a division of Pfizer Inc.*
Principal Display Panel (10 Vial Carton)
Geodon for Injection is a sterile medication used for intramuscular use only. It contains ziprasidone mesylate, equivalent to 20mg/mL of ziprasidone. Each mL (when reconstituted) contains 20 mg of ziprasidone and 4.7 mg of methanesulfonic acid solubilized by 294 mg of sulfobutyl ether B-cyclodextrin sodium (SBECD). It is advised to keep the medication between 15°C to 30°C (59°F to 86°F) and protect it from light. The duration of storage after reconstitution when protected from light is up to 24 hours at 15°C to 30°C (59°F to 86°F) or up to 7 days refrigerated, 2°C to 8°C (36°F to 46°F). Please refer to accompanying prescribing information for correct usage and dosage.*
Geodon 08a
Geodon 08b
This is a product description of Geodon for injection. It is provided in 10 single-dose vials, each equivalent to 20 mg/mL of ziprasidone mesylate. It should be stored protected from light and is intended solely for intramuscular use. The product is sterile and an NDC 0049-3920-10 is available. The dosage and use information provides instructions for reconstitution, with storage at controlled room temperature for up to 24 hours or refrigerated for up to 7 days. The product is distributed by Roerig and intended for intramuscular use only.*
Principal Display Panel (20 mg Capsule Bottle Label)
This is medication information for Geodon (ziprasidone HCI) capsules. Each capsule contains 20mg of ziprasidone hydrochloride monohydrate. It should be stored at 25°C (77°F), with permissible excursions to 15°C 10 30°C (59°F to 86°F), as controlled room temperature. For dosage and usage, refer to the accompanying prescribing information. It is distributed by Roerig, a division of Pfizer Inc and made in Ireland. The text also includes the UPC, NDC, lot, and GTIN info.*
Principal Display Panel (40 mg Capsule Bottle Label)
Principal Display Panel (60 mg Capsule Bottle Label)
This text is a product label for Geodon® (ziprasidone HCI) capsules containing 60mg of ziprasidone. The recommended storage temperature is 25°C (77°F), with deviations allowed between 15°C-30°C (59°F to 86°F). It also provides information about the manufacturer and distributor, including their addresses. Dosage information is not provided, and the text directs readers to the accompanying prescribing information.*
Principal Display Panel (80 mg Capsule Bottle Label)
This is a prescription medication called Geodon (ziprasidone HCI) that comes in capsules of 80mg. Each capsule contains Zprasidone hydrochloride monohydrate equivalent to 0.80g ziprasidone. The medication should be stored at 25°C, with excursions (temporary fluctuations) permitted to 15°C-30°C. More information about dosage and use can be found in the accompanying prescribing information. The medication is distributed by Roerlg, a division of Pfizer Inc, and is made in Ireland. The product has a Universal Product Code (UPC) of 800300490058605, a National Drug Code (NDC) of 0049-0058-60, and a lot number of z/EXP.*
Principal Display Panel (20 mg Capsule Bottle Label)
This is a description of a drug called Geodon, which comes in capsule form with 60 units in a pack. The drug contains ziprasidone monohydrate hydrochloride, which is equivalent to 20 mg of ziprasidone. The drug should be stored at a temperature between 15°C and 30°C (59°F to 86°F). The drug manufacturer is Roerig, a division of Pfizer Inc, New York, NY. The drug packaging has an NDC number of 0049-0352-60 and a GTIN number. The rest of the text is illegible due to errors.*
Principal Display Panel (40 mg Capsule Bottle Label)
Geodon® (ziprasidone) is a medication that comes in capsule form and is manufactured in Ireland. Each capsule contains 0.40 g of ziprasidone hydrochloride monohydrate, which is equivalent to ziprasidone. It is distributed by Roerig, a division of Pfizer Inc. in New York. The medication should be stored at 25°C (77°F), and excursions are allowed to 15°C to 30°C (59°F to 86°F). For dosage and usage information, please refer to the accompanying prescribing information. The lot number and expiration date are not available from the provided text.*
Principal Display Panel (60 mg Capsule Bottle Label)
This text is a medication label containing information about the storage conditions, dosage, manufacturer, and ingredients of Ziprasidone hydrochloride, marketed as Geodon. The medication is distributed by Roerig, a division of Pfizer, Inc., and each capsule contains 0.60 g of ziprasidone. The medication is meant for prescription use only and the prescribing information should be reviewed before using it. It is made in Ireland, and the label has barcodes for FPO, UPC, GTIN, and NDC. The storage temperature for this medication is 25°C, with permissible excursions between 15°C to 30°C, and the label provides reference to the USP Controlled Room Temperature guidelines.*
Principal Display Panel (80 mg Capsule Bottle Label)
This is a description of the storage conditions and dosage information for Geodon capsules. The capsules contain ziprasidone hydrochloride and are distributed by Roerig, a division of Pfizer Inc. The recommended storage temperature is 25°C (77°F), with permitted excursions to 15°C to 30°C (59°F to 86°F), as specified by USP controlled room temperature guidelines. Further dosage and usage information is available in the accompanying prescribing information. The text also contains product identification codes and a lot/expiry number. Made in Ireland.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.