Bromfenac Solution/ Drops
Product Images NDC 68083-313

3 FDA label images from Gland Pharma Limited · 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 Bromfenac (NDC 68083-313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma 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

Bromfenac-spl-carton.jpg (Bromfenac Spl Carton)

Bromfenac-spl-carton.jpg (Bromfenac Spl Carton)
Bromfenac Ophthalmic Solution 0.09% (once daily) 1.7 mL dropper bottle label from Gland Pharma Limited. The label identifies it as a topical ophthalmic solution for application in the eye. It includes active ingredient bromfenac 0.9 mg per mL, preservative benzalkonium chloride, and directions for use. The NDC is 68083-313-01.*
FDA Label Image

Bromfenac-spl-container.jpg (Bromfenac Spl Container)

Bromfenac-spl-container.jpg (Bromfenac Spl Container)
Label for Bromfenac Ophthalmic Solution 0.09% (0.9 mg/mL), a 1.7 mL drop solution for topical eye application. The label shows storage instructions (15° to 25°C), manufacturer details (Gland Pharma Limited, Hyderabad, India), and includes a barcode with lot and expiration information on the varnish area.*
FDA Label Image

Bromfenac-spl-structure (Bromfenac Spl Structure)

Bromfenac-spl-structure (Bromfenac Spl Structure)
Chemical structure of bromfenac, the active ingredient in BROMFENAC ophthalmic solution. The structure shows a brominated biphenyl compound with amide and carboxylate sodium salt groups, along with water of hydration (1.5 molecules).*

* 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.