Loxapine Capsule
Product Images NDC 70518-0416

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Loxapine (NDC 70518-0416). 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

Loxapine 50mg 70518 0416 00

Loxapine 50 mg oral capsules label showing quantity of 30 capsules. The label includes the NDC number 70518-0416-00, manufacturer information (Actavis, Sunrise, FL), barcode, and advisory to keep medication out of reach of children. The label also references storage conditions and repackaging by RemedyRepack Inc.*

FDA Label Image

Loxapine 50mg 70518 0416 01

Label of Loxapine 50 mg oral capsules showing a quantity of 100 capsules. The label includes the proprietary and generic name Loxapine, manufactured by RemedyRepack Inc. It displays the NDC number 70518-0416-01 and storage instructions with a note to see the package insert for directions.*

FDA Label Image

Loxapine 50mg 70518 0416 02

Loxapine 50 mg oral capsule label by RemedyRepack Inc. The label includes the drug name, strength, dosage form, quantity of 1 capsule, and barcode. Manufacturer listed as Actavis, Sunrise, FL. It contains regulatory information including NDC number 70518-0416-02, storage instructions, repackaging details, and a QR code.*

FDA Label Image

Image 1

Chemical structure of Loxapine, displaying its molecular framework with nitrogen, chlorine, and other elements indicated, labeled as LOXAPINE BASE.*

* 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.