Diclofenac Sodium
Product Images NDC 35356-714

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium (NDC 35356-714). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quality Care Products 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

75mg

75mg
Diclofenac Sodium DR 75 mg is a medication distributed by Rising Pharma Holdings, Inc. It comes in a package of 90 tablets each containing diclofenac sodium. The GTIN number is 00335356714906 and the NDC number is 35356-714-90. The medication should be stored at 68-77 degrees F and dispensed with a medication guide. The manufacturing company is Unique Pharmaceuticals Laboratories in Mumbai, India. The medication should be kept out of reach of children.*
FDA Label Image

Image Description (Diclofenacsodiumdr50mgunique)

Image Description (Diclofenacsodiumdr50mgunique)
This is a description of a medication called Diclofenac Sodium that comes in a 90-tablet package distributed by Mewze Pfldm. The tablets are brown and round and have "P;50 73" imprinted on them. The package has a warning about keeping the medication away from children and about the recommended storage temperature. The manufacturer of the medication is Unique Pharmaceutical Laboratories, which is a division of J.B. Chemicals and Pharmaceuticals Ltd. located in Mumbai, India. There is serial number, lot number, and expiration date information provided as well.*
FDA Label Image

Diclofenac Structure (Diclofenac Structure)

* 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.