Olanzapine Structural Formula (80d4f225 B719 4668 99aa 50b106065646 01)
Olanzapine
Product Images NDC 68258-7153
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 68258-7153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Dispensing Solutions, 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.
Ndc 68258-7152-xx (Ndc 68258 7152 Xx Teva)
This is a description of a medication with the brand name TEVA. The medication is an off-white, round, film-coated tablet that is debossed with "TEVA" and "5767". Each tablet contains 2.5mg of Olanzapine. The medication is dispensed with a medication guide and cautionary measures should be taken such as keeping it out of reach of children and storing it in a tightly sealed and light-resistant container. The lot number is "SAMPLE" with an expiration date of "00-00". This product is intended for prescription and can only be distributed to the patient it was prescribed to.*
Ndc 68258-7153-xx (Ndc 68258 7153 Xx Teva)
This is a bottle of Olanzapine 15mg tablets manufactured by Teva Pharmaceuticals in Sellersville, PA. Each bottle contains XX tablets with product number PY7153-X and NDC number 68258-7153-XX. The tablets are blue, capsule-shaped, and film-coated with the "Teva" logo and "6771" debossed on them. They are to be taken orally, prescribed only for the patient named on the Rx #30000659 label, and should be kept out of the reach of children. The lot number is "Sample" with an expiration date of "00-00". The product should be stored at 68 to 77 °F, and it is recommended to follow USP for storage.*
Ndc 68258-7154-xx (Ndc 68258 7154 Xx Teva)
This is a pharmaceutical product that contains Olanzapine, an antipsychotic drug. The product is manufactured by Teva Pharmaceuticals USA in Sellersville, PA 18960. The product ID is an off-white round film-coated tablet debossed with TEVA/6769. The bulk source National Drug Code (NDC) is 00093-5769-01, and the NDC for the individual product is 68258-7154-XX. Each tablet contains 7.5mg of OlanzapineUSP. The product is meant to be taken orally, once a day as directed by a doctor. There are some side effects such as dizziness, weight gain, or constipation, and patients should use caution while driving or performing other tasks that require mental alertness. Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. The product should be kept out of children's reach and stored at 68°- 77° F. There is more information available in the full prescribing information.*
* 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.
