Diclofenac Potassium Tablet, Film Coated
Product Images NDC 60290-088

3 FDA label images from Umedica Laboratories Usa Inc. · 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 Diclofenac Potassium (NDC 60290-088). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Umedica Laboratories Usa 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

Hdpe Bottle Of 1000s (Diclofenac Potassium 1000s Label)

Hdpe Bottle Of 1000s (Diclofenac Potassium 1000s Label)
Label for Diclofenac Potassium Tablets USP 50 mg film-coated tablets, oral use, from Umedica Laboratories USA Inc. The label includes storage instructions, usual dosage reference, a barcode, and a package count of 1000 tablets. The label indicates the product is prescription only (Rx only).*
FDA Label Image

Hdpe Bottle Of 100s (Diclofenac Potassium 100s Label)

Hdpe Bottle Of 100s (Diclofenac Potassium 100s Label)
Label for Diclofenac Potassium Tablets USP 50 mg film-coated tablets by Umedica Laboratories USA Inc. The label includes storage instructions, a note that the package is child-resistant, and states it contains 100 tablets. Manufactured by Umedica Laboratories Pvt. Ltd. in Gujarat, India, the label also features an NDC number 60290-057-01 and a barcode.*
FDA Label Image

Diclofenac Potassium (Diclofenac Potassium)

Diclofenac Potassium (Diclofenac Potassium)
Chemical structure diagram of Diclofenac Potassium showing the arrangement of aromatic rings and functional groups including carboxylate and chlorine substituents.*

* 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.