Meloxicam Tablet
Product Images NDC 65862-098

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 65862-098). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (7.5 mg (100 Tablet Bottle))

Package Label-principal Display Panel (7.5 mg (100 Tablet Bottle))
Label for Meloxicam Tablets, USP 7.5 mg, a drug for further processing supplied by Aurobindo Pharma Limited. The label includes the NDC 65862-097-01, states 100 tablets per container, distribution information for Aurobindo Pharma USA, Inc., storage instructions, and a note that the Medication Guide must be dispensed with the product. The label also mentions the product is made in India.*
FDA Label Image

Package Label-principal Display Panel (15 mg (100 Tablet Bottle))

Package Label-principal Display Panel (15 mg (100 Tablet Bottle))
Label for Meloxicam Tablets, USP 15 mg by Aurobindo Pharma Limited. The label states the contents per tablet, storage instructions, and dispenser warnings. It specifies a 100 tablet count and includes distributor information with a barcode.*
FDA Label Image

Chemical Structure (Meloxicam Str)

Chemical Structure (Meloxicam Str)
Chemical structure of Meloxicam, showing its molecular arrangement including aromatic rings, sulfur, oxygen, nitrogen atoms, and methyl groups, consistent with its designation as the active ingredient in the drug.*

* 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.