Olanzapine Tablet, Film Coated
Product Images NDC 60429-621

7 FDA label images from Golden State Medical Supply, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 60429-621). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, Inc., 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

60429-620-30lb (OLANZAPINE 2.5MG TABS.jpg)

60429-620-30lb (OLANZAPINE 2.5MG TABS.jpg)
Label for Olanzapine tablets, USP, 2.5 mg strength, containing 30 tablets. The label displays the NDC number 60429-620-30 and notes the product is for oral use only. The labeler is Golden State Medical Supply, Inc. Storage instructions and barcode are also visible on the label.*
FDA Label Image

60429-621-30lb (OLANZAPINE 5MG TABS.jpg)

60429-621-30lb (OLANZAPINE 5MG TABS.jpg)
Label for Olanzapine tablets, USP, 5 mg strength, containing 30 film-coated tablets. The label shows the NDC number 60429-621-30 and indicates the product is for oral use. The labeler is Golden State Medical Supply, Inc., with storage instructions and a note to see the package insert for dosage information. The label also includes a barcode and space for lot number, expiration date, and serial number.*
FDA Label Image

60429-622-30lb Olanzapine 7.5mg Tabs.jpg (60429 622 30lb Olanzapine 7.5mg Tabs)

60429-622-30lb Olanzapine 7.5mg Tabs.jpg (60429 622 30lb  Olanzapine 7.5mg Tabs)
Label for Olanzapine tablets USP 7.5 mg, film-coated oral tablets. The package contains 30 tablets. Labeler is Golden State Medical Supply, Inc. The label includes NDC number 60429-622-30, storage instructions, and a note to see the package insert for dosage information. It is marked for prescription use only (Rx only).*
FDA Label Image

60429-623-30lb Olanzapine 10mg Tabs.jpg (60429 623 30lb Olanzapine 10mg Tabs)

60429-623-30lb Olanzapine 10mg Tabs.jpg (60429 623 30lb  Olanzapine 10mg Tabs)
Label for Olanzapine 10 mg tablets, USP, containing 30 tablets per bottle. The label includes the NDC number 60429-623-30, and is marked for prescription use only (Rx only). It shows storage instructions and a barcode. The labeler is identified as Golden State Medical Supply, Inc.*
FDA Label Image

60429-624-30lb Olanzapine 15mg Tabs.jpg (60429 624 30lb Olanzapine 15mg Tabs)

60429-624-30lb Olanzapine 15mg Tabs.jpg (60429 624 30lb  Olanzapine 15mg Tabs)
Label for Olanzapine tablets USP, 15 mg strength, with a package quantity of 30 tablets. The label includes the NDC 60429-624-30 and indicates the product is for prescription use only (Rx only). The labeler is GSMS Incorporated, also shown as Golden State Medical Supply, Inc. Additional storage and handling instructions are included on the label.*
FDA Label Image

60429-625-30lb Olanzapine 20mg Tabs.jpg (60429 625 30lb Olanzapine 20mg Tabs)

60429-625-30lb Olanzapine 20mg Tabs.jpg (60429 625 30lb  Olanzapine 20mg Tabs)
Label for Olanzapine 20 mg tablets, USP, issued by Golden State Medical Supply, Inc. The label shows the NDC 60429-625-30 and indicates a package count of 30 tablets. The text includes storage instructions and a barcode, with 'Rx only' prominently displayed. The label also features the manufacturer information and a reminder to see the package insert for dosage information.*
FDA Label Image

Structure (Olanzapineusp)

Structure (Olanzapineusp)
Chemical structure of Olanzapine, showing the molecular arrangement including a thienobenzodiazepine core with a piperazine side chain and methyl substitutions.*

* 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.