Meloxicam Tablet
Product Images NDC 61442-127

7 FDA label images from Carlsbad Technology, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Meloxicam (NDC 61442-127). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Carlsbad Technology, 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

Structural Formula (Mel01 0005 01)

Structural Formula (Mel01 0005 01)
Chemical structure of Meloxicam, showing its molecular arrangement with labeled atoms and bonds consistent with the nonproprietary drug ingredient Meloxicam.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 02)

Package Label – Principal Display Panel (Mel01 0005 02)
Label for Meloxicam 7.5 mg tablets, USP, an oral prescription drug by Carlsbad Technology, Inc. The label states each tablet contains 7.5 mg Meloxicam, with a package size of 30 tablets. Storage instructions specify 20° to 25°C. The label includes dispensing warnings and manufacturer details in Taichung, Taiwan, and distribution information from Carlsbad, CA, USA.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 03)

Package Label – Principal Display Panel (Mel01 0005 03)
Meloxicam 7.5 mg Tablets, USP label for oral use, produced by Carlsbad Technology, Inc. The label includes storage instructions, dispensing guidelines, and warns to keep out of reach of children. The package contains 100 tablets. NDC 61442-126-01 is shown along with manufacturer and distributor information.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 04)

Package Label – Principal Display Panel (Mel01 0005 04)
Meloxicam 7.5 mg tablets, USP oral dosage form. The label shows the product strength as 7.5 mg per tablet and indicates prescription use only (Rx Only). It includes storage instructions to keep tablets in a dry place at 20° to 25°C and warnings to keep out of reach of children. The labeler is Carlsbad Technology, Inc., with a package size of 1000 tablets. Manufacturing and distribution information is also visible, along with the NDC 61442-126-10.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 05)

Package Label – Principal Display Panel (Mel01 0005 05)
Label for Meloxicam 15 mg oral tablets, USP, manufactured by Carlsbad Technology, Inc. The label shows product name, strength (15 mg), quantity (30 tablets), and storage instructions. It includes dispensing warnings and manufacturer details with barcode and lot/expiration date fields.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 06)

Package Label – Principal Display Panel (Mel01 0005 06)
Label for Meloxicam 15 mg oral tablets, USP, by Carlsbad Technology, Inc. The label indicates a prescription-only product with a package size of 100 tablets. Storage instructions specify controlled room temperature between 20° to 25°C. The label includes dispensing warnings and manufacturer details from Taiwan and the USA, along with NDC 61442-127-01.*
FDA Label Image

Package Label – Principal Display Panel (Mel01 0005 07)

Package Label – Principal Display Panel (Mel01 0005 07)
Label for Meloxicam Tablets, USP 15 mg oral tablets by Carlsbad Technology, Inc. The label includes dosage storage instructions, a note that the medication guide must be dispensed with the product, and the quantity of 1000 tablets. Manufacturer and distributor information in Taiwan and the USA are also shown, along with an NDC number and barcode.*

* 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.