Meloxicam
Product Images NDC 69336-101

3 FDA label images from Sterling Knight Pharmaceuticals, Llc · 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 69336-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sterling Knight 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

Image1 (Meloxi1)

Image1 (Meloxi1)
Meloxicam 7.5 mg Tablets, USP label by Sterling Knight Pharmaceuticals, LLC. The label indicates the tablet strength as 7.5 mg with a package count of 30 tablets. It includes storage instructions to keep the product at 20°C to 25°C and dispense in a tight container, along with a barcode and NDC 69336-101-30. The label also notes that the medication guide must accompany the product and states it is Rx only.*
FDA Label Image

Image2 (Meloxi2)

Image2 (Meloxi2)
Meloxicam 15 mg Tablets, USP label from Sterling Knight Pharmaceuticals, LLC. The label shows a 30-tablet package with prescription-only status. Storage instructions specify keeping tablets at 20° to 25°C in a dry place and out of reach of children. The label includes the NDC number 69336-102-30 and a barcode.*
FDA Label Image

Struct (Structure)

Struct (Structure)
Chemical structure diagram of meloxicam, showing its molecular framework with distinct functional groups including a thiazole ring and sulfonamide moiety, consistent with the active ingredient meloxicam from Sterling Knight Pharmaceuticals.*

* 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.