Diclofenac Potassium Capsule, Liquid Filled
Product Images NDC 64380-841

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Potassium (NDC 64380-841). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science 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.

FDA Label Image

Structural Formula (653e79de D7ae 4ccb B567 C8162a09bba4 01)

Chemical structure diagram of diclofenac potassium showing its molecular arrangement with labeled chemical groups including potassium (K), two chlorine (Cl) atoms, and carboxylate group (CH2COO).*

FDA Label Image

Figure 1 (653e79de D7ae 4ccb B567 C8162a09bba4 02)

This is a line graph depicting mean pain intensity over a 48-hour period for diclofenac potassium 25 mg (Zipsor) compared to placebo. The x-axis shows dosing intervals from baseline to the end of 48 hours, while the y-axis indicates pain intensity on a scale from 0 (no pain) to 10 (worst pain). Two lines represent mean pain scores: one for diclofenac potassium 25 mg and one for placebo.*

FDA Label Image

25 mg 100-count Bottle Label (653e79de D7ae 4ccb B567 C8162a09bba4 03)

Label for Diclofenac Potassium Capsules 25 mg, liquid-filled oral capsules. The label shows the active ingredient diclofenac potassium at 25 mg strength. It is manufactured by Strides Pharma Science Limited, Bengaluru, India, and distributed by Strides Pharma Inc., East Brunswick, NJ. The package contains 100 capsules and indicates prescription use only. Storage instructions and dosage guidance are also visible on the label.*

* 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.