Bromfenac Solution/ Drops
Product Images NDC 68180-434

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Bromfenac (NDC 68180-434). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Figure 1 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 01)

Figure 1 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 01)
Chemical structure of bromfenac monohydrate showing brominated aromatic rings and sodium carboxylate and amine functional groups.*
FDA Label Image

Figure A (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 02)

Figure A (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 02)
An instructional diagram showing two steps of breaking the tamper-evident ring on a small ophthalmic dropper bottle. The first image illustrates the tamper-evident ring intact, with a hand grasping the cap. The second image shows the ring broken after twisting the cap, indicating the bottle is opened.*
FDA Label Image

Figure B (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 03)

Figure B (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 03)
An instructional illustration showing a hand removing or twisting off the cap of an ophthalmic solution bottle, labeled as Figure B. The image demonstrates how to open the dropper bottle before use.*
FDA Label Image

Figure C (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 04)

Figure C (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 04)
An instructional illustration labeled Figure C showing hands removing or twisting the cap of an ophthalmic drop bottle, demonstrating how to open the product bottle for use.*
FDA Label Image

Figure D (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 05)

Figure D (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 05)
An instructional illustration labeled Figure D depicts a hand holding an eye drop bottle, with an arrow indicating the motion to twist or rotate the dropper tip. This image likely demonstrates part of the usage instructions for an ophthalmic solution.*
FDA Label Image

Figure E (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 06)

Figure E (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 06)
An instructional illustration labeled Figure E showing hands demonstrating how to invert an ophthalmic dropper bottle, likely as part of usage directions for BROMFENAC ophthalmic solution 0.75 mg/mL by Lupin Pharmaceuticals.*
FDA Label Image

Figure F (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 07)

Figure F (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 07)
An instructional illustration labeled Figure F showing two hands. One hand holds a small bottle upright while the other hand is positioned below it, with an arrow indicating a twisting motion to remove or open the cap, likely demonstrating how to use an ophthalmic solution dropper bottle.*
FDA Label Image

Figure G (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 08)

Figure G (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 08)
An instructional illustration showing a person tilting their head back and administering eye drops into their eye with a dropper. The image emphasizes the proper technique for ophthalmic solution application.*
FDA Label Image

Figure 6 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 09)

Figure 6 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 09)
Label for Bromfenac Ophthalmic Solution 0.75 mg/mL, a topical eye drop solution in a 5 mL bottle. Manufactured by Lupin Pharmaceuticals, Inc., the label includes dosing strength, usage indication for the eye, and space for lot and expiration date printing. The product is prescription-only.*
FDA Label Image

Figure 7 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 10)

Figure 7 (Ef3792bb 0d03 450c B4fa 53fbaae49bd5 10)
Label for Bromfenac Ophthalmic Solution 0.075% sterile drops in 5 mL packaging by Lupin Pharmaceuticals, Inc. The label highlights topical use in the eye and includes active ingredient details, storage instructions, and manufacturer information in Baltimore, Maryland, and India. The NDC is 68180-434.*

* 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.