Olanzapine Tablet, Orally Disintegrating
Product Images NDC 69452-562

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 69452-562). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bionpharma 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

Structure (Olanzapine Odt Figure 1)

Chemical structure of olanzapine depicted as a molecular diagram showing its heterocyclic and aromatic rings with nitrogen, sulfur atoms, and methyl groups.*

FDA Label Image

Label1 (Olanzapine Odt Figure 2)

The label for olanzapine orally disintegrating tablets USP, 5 mg strength, shows a package of 30 tablets. The label indicates the product is for oral use, dispensed by Bionpharma Inc., with storage instructions and child-resistant packaging. It also notes that each tablet contains 5 mg olanzapine USP and includes warnings about phenylketonurics and medication handling.*

FDA Label Image

Label2 (Olanzapine Odt Figure 3)

Label for olanzapine orally disintegrating tablets, USP, 10 mg strength, containing 30 tablets per bottle. The label includes the NDC number 69452-562-13 and instructions advising the pharmacist to dispense the medication guide. It notes phenylketonurics content, storage conditions, and warnings to keep out of reach of children. The product is manufactured by Bionpharma Inc., made in India.*

FDA Label Image

Label3 (Olanzapine Odt Figure 4)

Label for Olanzapine Orally Disintegrating Tablets, USP 15 mg by Bionpharma Inc. The label states it contains 30 tablets and provides dosage information and storage instructions. It notes the product is made in India and includes a pharmacist dispensing instruction with a website link for medication guidance.*

FDA Label Image

Label4 (Olanzapine Odt Figure 5)

Label for olanzapine orally disintegrating tablets, USP 20 mg strength. The 30-tablet container is labeled for oral use and is distributed by Bionpharma Inc. Features include child-resistant packaging instructions, storage conditions (20 to 25°C), and a warning to keep out of reach of children. The label notes the presence of phenylalanine in each tablet and directs to accompany literature for dosage 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.