Meloxicam
Product Images NDC 50436-1125

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 50436-1125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

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

Chemical Structure (33e59d34 E3bd 4b74 Bbba 1fc10df4af8e 01)
Chemical structure diagram of meloxicam, showing its molecular bonds and functional groups, including heterocyclic rings and sulfonamide components.*
FDA Label Image

Unichem Logo (33e59d34 E3bd 4b74 Bbba 1fc10df4af8e 02)

FDA Label Image

Image (8d582aa1 Bdad 4021 Bff1 1cff1f59e376 954 2)

FDA Label Image

Label Image (Lbl504361124)

Label Image (Lbl504361124)
Meloxicam 7.5 mg / 30 tablets packaging label showing the active ingredient meloxicam USP 7.5 mg. The label includes storage instructions, warnings, and medication guide advisories. It also identifies the manufacturer as Unichem Laboratories Ltd. located in Goa, India, and the labeler as Unit Dose Services, LLC, Dania, FL. Lot number, expiration date, and barcode information are present but not fully legible.*
FDA Label Image

Label Image (Lbl504361125)

Label Image (Lbl504361125)
Meloxicam 15 mg tablet unit dose carton from Unit Dose Services. The label states each tablet contains Meloxicam USP 15 mg, with 30 tablets per package. It includes storage instructions to keep in a dry place at controlled room temperature, a pharmacist dispensing note, and labeler information for Unichem Laboratories Ltd, Dania, FL.*

* 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.