Bromfenac Solution/ Drops
Product Images NDC 72266-142

3 FDA label images from Fosun Pharma Usa Inc. · 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 72266-142). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fosun Pharma Usa Inc., 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-carton.jpg (Bromfenac Carton)

Bromfenac-carton.jpg (Bromfenac Carton)
Bromfenac Ophthalmic Solution 0.09% (.9 mg/mL) in a 1.7 mL bottle for topical application in the eye. The label shows the product name, strength, route (ophthalmic), and dosage frequency (once daily). It is labeled as prescription-only (Rx Only) and distributed by Fosun Pharma USA Inc., made in India. Additional text includes active and inactive ingredients, dosage instructions, storage conditions, and a barcode.*
FDA Label Image

Bromfenac-label.jpg (Bromfenac Label)

Bromfenac-label.jpg (Bromfenac Label)
Label for BROMFENAC 0.09% ophthalmic solution, a prescription eye drop distributed by Fosun Pharma USA Inc. The label includes storage instructions (store at 15° to 25°C), container volume of 1.7 mL, and indicates the product is for topical application in the eye. The label also shows the NDC code 72266-142-01, a barcode, and space for batch details and expiration date.*
FDA Label Image

Bromfenac-structure.jpg (Bromfenac Structure)

Bromfenac-structure.jpg (Bromfenac Structure)
Chemical structure of bromfenac, showing a bromine-substituted aromatic ring connected via a carbonyl group to an aminobenzoic acid derivative with a sodium acetate moiety and 1.5 molecules of water.*

* 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.