Diclofenac Sodium Tablet, Delayed Release
Product Images NDC 63187-761

3 FDA label images from Proficient Rx Lp · 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 Sodium (NDC 63187-761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

63187-761-15 (63187 761 15)

63187-761-15 (63187 761 15)
Packaging label for Diclofenac Sodium 75 mg delayed release tablets by Proficient Rx LP. The label indicates a count of 15 DR tablets, with each enteric-coated tablet containing 75 mg Diclofenac Sodium USP. The label includes product ID PD076115, manufacturer Actavis Elizabeth LLC, and storage information at 25°C (77°F). It also notes to keep medication out of children’s reach and has multiple smaller labels listing lot, expiration, and NDC 63187-761-15.*
FDA Label Image

78e77986-figure-01 (Diclofenac Sodium Dr Tablets Usp 1)

78e77986-figure-01 (Diclofenac Sodium Dr Tablets Usp 1)
Chemical structure of Diclofenac Sodium showing two chlorinated benzene rings linked by an amino group, with a sodium carboxylate side chain attached.*
FDA Label Image

78e77986-figure-03 (Diclofenac Sodium Dr Tablets Usp 3)

78e77986-figure-03 (Diclofenac Sodium Dr Tablets Usp 3)
The packaging label for Diclofenac Sodium 75 mg delayed-release tablets shows a white rectangular blister pack containing 10 tablets arranged in two rows of five. The label printed on the blister includes the product name, strength (75 mg), dosage form (delayed-release tablets), and the manufacturer Proficient Rx LP.*

* 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.