Meloxicam Tablet
Product Images NDC 70518-0039

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Meloxicam (NDC 70518-0039). 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 (Meloxicam 7.5mg 70518 0039 01)

Meloxicam 7.5 mg oral tablet label showing a quantity of 30 tablets. The label includes the brand 'remedy repack' and states the product is RX only. It lists the NDC number 70518-0039-01, manufacturer Unichem Pharma, Inc. in Rochelle Park, NJ, and repackager RemedyRepack Inc. in Indiana, PA. Storage conditions and a QR code are also visible.*

FDA Label Image

Meloxicam 7.5mg 70518 0039 02

Label for meloxicam 7.5 mg oral tablets, quantity of 90, repackaged by RemedyRepack Inc. The label includes the NDC number 70518-0039-02, manufacturer Unichem Pharma, Inc. (Rochelle Park, NJ), and storage instructions. A QR code and barcode are also visible on the label.*

FDA Label Image

Meloxicam 7.5mg 70518 0039 03

Meloxicam 7.5 mg tablet packaging label showing a quantity of 20 tablets. The label features the brand name RemedyRepack, includes the NDC number 70518-0039-03, and lists Unichem Pharma, Inc. as the manufacturer in Rochelle Park, NJ. Directions for use refer to the package insert.*

FDA Label Image

Remedy_label (Remedy Label)

Label for meloxicam 7.5 mg oral tablets, quantity of 40, repackaged by RemedyRepack Inc. The label includes the NDC 70518-0039-00, directions to see the package insert, storage instructions, and manufacturer information for Unichem Pharma, Inc., Rochelle Park, NJ. The label also displays a barcode and a QR code.*

* 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.