Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 72336-432

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Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diclofenac Potassium (NDC 72336-432). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifsa Drugs 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

Diclofenac Potassium (72336432 1)

Diclofenac Potassium (72336432 1)
Label for Diclofenac Potassium Capsules 25 mg, liquid-filled oral capsules in a 120-capsule package. The label shows NDC 72336-432-12, distributed by Lifsa Drugs LLC and manufactured by Strides Pharma Science Ltd., India. Includes dosage and storage instructions, pharmacist dispensing warning, and barcodes.*
FDA Label Image

Figure 1 (Figure 1)

Figure 1 (Figure 1)
A line graph titled 'Mean Pain Intensity Scores at the Midpoint and End of Each Dose Interval in Postbunionectomy Pain Study 1' showing mean pain intensity over nine dosing intervals for two groups: 25 mg Zip­sor and placebo. The y-axis represents mean pain intensity from 0 to 10, and the x-axis shows time points from baseline through end of dose 9. The 25 mg Zip­sor group is indicated with a dashed line and triangles, showing lower pain scores compared to the placebo group, depicted with a solid line and circles.*
FDA Label Image

Logo (Lifsa Logo 1)

FDA Label Image
FDA Label Image

Chemical Structure (Structure)

Chemical Structure (Structure)
Chemical structure of diclofenac potassium, showing two benzene rings connected by a nitrogen atom, with two chlorine atoms on one ring and a potassium carboxylate group attached to the other.*

* 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.