Meloxicam
Product Images NDC 33261-071

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Meloxicam (NDC 33261-071). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aidarex Pharmaceuticals Llc, 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 (Meloxicam Tabs Unichem 1)

Structure (Meloxicam Tabs Unichem 1)
Chemical structure of meloxicam, showing its molecular formula with ring and heterocyclic features including sulfonamide and thiazole groups.*
FDA Label Image

Company Logo (Meloxicam Tabs Unichem 2)

FDA Label Image

Company Logo (Meloxicam Tabs Unichem 3)

FDA Label Image

Image Label (Meloxicam Tabs Unichem 4)

Image Label (Meloxicam Tabs Unichem 4)
Meloxicam 7.5 mg tablets packaging label showing a package of 90 tablets by Aidarex Pharmaceuticals LLC. The label indicates the active ingredient meloxicam at 7.5 mg per tablet. It includes directions fields for dosage and frequency, and states it is a generic for Mobic with NDC 33261-0070-90. The manufacturer is Unichem Laboratories Ltd., Goa, India.*
FDA Label Image

Image Label (Meloxicam Tabs Unichem 5)

Image Label (Meloxicam Tabs Unichem 5)
Meloxicam 15 mg tablet label from Aidarex Pharmaceuticals LLC. The label states each tablet contains 15 mg of the active ingredient meloxicam. The package contains 90 tablets. The label includes NDC 33261-0071-90 and RX number 1000802612. It also notes the product is a generic for Mobic and is manufactured by Unichem Laboratories Ltd. Goa, India.*

* 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.