Zyprexa
Product Images NDC 0002-4112

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Zyprexa (NDC 0002-4112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eli Lilly And Company, 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

Package Label (ZYPREXA 10 mg tablet, bottle of 30)

Package Label (ZYPREXA 10 mg tablet, bottle of 30)
The label for Zyprexa Olanzapine Tablets by Eli Lilly and Company shows a package containing 30 tablets, strength 10 mg. The label includes instructions that it is Rx only, with medication guide dispensing information. Storage instructions and warnings about the integrity of the inner seal are also present.*
FDA Label Image

Package Label (ZYPREXA 15 mg tablet, bottle of 30)

Package Label (ZYPREXA 15 mg tablet, bottle of 30)
Zyprexa 15 mg tablets packaging label containing 30 tablets by Eli Lilly and Company. The label displays the proprietary name with the dosage strength prominently in a blue box, the active ingredient Olanzapine, along with instructions for storage and a barcode. The label also includes a warning not to use if the inner seal is missing or broken.*
FDA Label Image

Package Label (ZYPREXA 20 mg tablet, bottle of 30, trade)

Package Label (ZYPREXA 20 mg tablet, bottle of 30, trade)
Zyprexa 20 mg tablets packaging label showing the brand name, active ingredient Olanzapine, tablet strength of 20 mg, and a count of 30 tablets. The label includes the Eli Lilly logo, a pink tablet imprint, and important storage instructions. The product is marked Rx only and includes a barcode and NDC number 0002-4420-30.*
FDA Label Image

Package Label (ZYPREXA 2.5 mg tablet, bottle of 30)

Package Label (ZYPREXA 2.5 mg tablet, bottle of 30)
Label for Zyprexa Olanzapine Tablets 2.5 mg, supplied in a package of 30 tablets. The label includes the brand name Zyprexa prominently, dosage strength, and prescription only status. It also notes that a medication guide should be dispensed to patients. The label features branding for Eli Lilly and Company, along with storage instructions and a barcode.*
FDA Label Image

Package Label (ZYPREXA 5 mg tablet, bottle of 30)

Package Label (ZYPREXA 5 mg tablet, bottle of 30)
Zyprexa 5 mg Olanzapine Tablets label from Eli Lilly and Company. The label indicates a package containing 30 tablets with NDC 0002-4115-30. The label highlights that this medication is Rx only and includes storage instructions, a barcode, and a warning about the integrity of the inner seal. The Lilly logo is present on the label.*
FDA Label Image

Package Label (ZYPREXA 7.5 mg tablet, bottle of 30)

Package Label (ZYPREXA 7.5 mg tablet, bottle of 30)
Zyprexa 7.5 mg Olanzapine Tablets package label showing the Eli Lilly and Company brand. The label indicates a bottle of 30 tablets with prescription use only. It includes warnings about the inner seal, storage instructions, and dispensing guidance. The label features barcodes, a QR code, and the product NDC 0002-4116-30.*
FDA Label Image

Chemical Structure (Zyprexa F001 V1)

Chemical Structure (Zyprexa F001 V1)
Chemical structure diagram of the active ingredient in Zyprexa, showing the molecular framework including nitrogen, sulfur, and methyl groups consistent with its chemical composition.*
FDA Label Image

Zyprexa Im 10mg Carton 213215 V2

Zyprexa Im 10mg Carton 213215 V2
Packaging label for Zyprexa IntraMuscular 10 mg/vial, an olanzapine injection. The sterile single-dose vial is for intramuscular use only and labeled Rx only. The label includes storage instructions before and after reconstitution, inactive ingredients, reconstitution details, and marketing information by Eli Lilly USA, LLC in Indianapolis, Indiana. The product is made in Ireland.*
FDA Label Image

Package Label (ZYPREXA ZYDIS 10 mg tablet, 30 sachets)

Package Label (ZYPREXA ZYDIS 10 mg tablet, 30 sachets)
Zyprexa Zydis 10 mg orally disintegrating tablets packaging label by Eli Lilly and Company. The label shows the product name, strength, dosage form, dosage instructions, and storage information. It includes a barcode, lot number, and clear branding with the Lilly logo. The product contains 30 tablets per box.*
FDA Label Image

Package Label (ZYPREXA ZYDIS 15 mg tablet, 30 sachets)

Package Label (ZYPREXA ZYDIS 15 mg tablet, 30 sachets)
Packaging label for Zyprexa Zydis 15 mg oral disintegrating tablets by Eli Lilly and Company. The label displays the brand name prominently with strength (15 mg) noted in large blue font. It includes storage instructions, a medication guide note, and usage instructions illustrations. The label indicates it contains olanzapine and warns to open the pouch immediately prior to use.*
FDA Label Image

Package Label (ZYPREXA ZYDIS 20 mg tablet, 30 sachets, trade)

Package Label (ZYPREXA ZYDIS 20 mg tablet, 30 sachets, trade)
Zyprexa Zydis 20 mg oral disintegrating tablets carton from Eli Lilly and Company. The packaging includes the product name, strength, dosage form, and instructions for use illustrated with icons. It states the active ingredient as olanzapine and has a barcode. The label also features the Lilly logo and dispensing directions.*
FDA Label Image

Package Label (ZYPREXA ZYDIS 5 mg tablet, 30 sachets)

Package Label (ZYPREXA ZYDIS 5 mg tablet, 30 sachets)
Packaging label for Zyprexa Zydis 5 mg orally disintegrating tablets from Eli Lilly and Company. The label includes the proprietary name Zyprexa Zydis, the strength of 5 mg, and indicates 30 sachets per package. Instructions for use and storage recommendations are visible, along with caution about phenylketonurics containing phenylalanine 0.34 mg per tablet.*

* 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.