Meloxicam Tablet
Product Images NDC 85534-0019

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Meloxicam (NDC 85534-0019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hawaii Repack, 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (33e59d34 E3bd 4b74 Bbba 1fc10df4af8e 01)

Chemical Structure (33e59d34 E3bd 4b74 Bbba 1fc10df4af8e 01)
Chemical structure of meloxicam, showing its molecular configuration with characteristic rings and functional groups typical of the active ingredient meloxicam.*
FDA Label Image

Image Description (Label 15mg)

Image Description (Label 15mg)
Four prescription labels for Meloxicam Tablets USP 15 mg, distributed by Hawaii Repack, Inc., Honolulu, HI. Each label shows different packaging quantities: 30, 60, 90, and 120 tablets. Manufactured for Unichem Pharmaceuticals (USA), Inc., the tablets are described as light yellow, oblong, biconvex, uncoated. Labels include QR codes, storage instructions, and cautionary statements about dispensing and child safety.*
FDA Label Image

Image Description (Label 7 5mg)

Image Description (Label 7 5mg)
Four separate labels for Meloxicam Tablets USP 7.5 mg in quantities of 30, 60, 90, and 120 tablets, distributed by Hawaii RePACK at 677 Ala Moana Blvd, Honolulu, HI. Each label includes the NDC, a QR code, drug status as prescription only, and storage instructions. The tablets are described as light yellow, oblong, biconvex, uncoated.*

* 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.