Olanzapine Injection, Powder, For Solution
Product Images NDC 0121-1072

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Olanzapine (NDC 0121-1072). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pai Holdings, Llc Dba Pai Pharma, 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

Chemical Structure (Olanzapine Inj 1)

Chemical Structure (Olanzapine Inj 1)
Chemical structure of olanzapine, showing its heterocyclic rings and methyl group substitutions as a two-dimensional molecular diagram.*
FDA Label Image

Olanzapine For Injection Carton Ndc 0121-1072-55 (Olanzapine Inj 2)

Olanzapine For Injection Carton Ndc 0121-1072-55 (Olanzapine Inj 2)
Packaging label for Olanzapine Intramuscular Injection, powder for solution, 10 mg per vial. The label includes dosage strength, instructions indicating single-dose vial and intramuscular use only, storage conditions, inactive ingredients, reconstitution instructions, and distributor information for PAI Pharma. The label also features barcodes and the PAI Pharma logo.*
FDA Label Image

Olanzapine For Injection Vial Ndc 0121-1072-55 (Olanzapine Inj 3)

Olanzapine For Injection Vial Ndc 0121-1072-55 (Olanzapine Inj 3)
Label for Olanzapine for Injection 10 mg/vial, an intramuscular injection powder for solution. The single-dose vial is labeled for use by PAI Holdings, LLC dba PAI Pharma, with the product NDC number 0121-1072-55. The label includes dosage and administration instructions reference, barcode, lot, and expiration date fields.*

* 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.