Loxapine Capsule
Product Images NDC 70518-1896

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Loxapine (NDC 70518-1896). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Loxapine 25mg 70518 1896 01)

Loxapine 25 mg oral capsules label repackaged by RemedyRepack Inc. The label shows a quantity of 100 capsules with NDC 70518-1896-01. Manufacturer is Lannett, Bohemia, NY. Directions refer to the package insert. Storage instructions and a QR code are also included.*

FDA Label Image

Mm3 (Loxapine 25mg 70518 1896 02)

Loxapine 25 mg capsule packaging label showing the quantity of 1 capsule. The label includes the NDC number 70518-1896-02, manufacturer information for Lannett in Bohemia, NY, and repackaging details by RemedyRepack Inc. It has directions for storage and usage instructions to see the package insert.*

FDA Label Image

Remedy_label (Remedy Label)

Loxapine 25 mg capsule packaging label by RemedyRepack Inc. The label shows a quantity of 30 capsules. It includes the NDC number 70518-1896-00 and a manufacturing location of Lannett, Bohemia, NY. It provides storage and repackaging information, along with a QR code and standard caution to keep medication out of children's reach. Directions reference the package insert.*

FDA Label Image

Loxapine-molec-structure (Loxapine Capsules Usp 1)

Chemical structure of Loxapine, showing its molecular framework including nitrogen, oxygen, and chlorine atoms as labeled in the diagram with the caption 'LOXAPINE BASE' below.*

* 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.