Moxifloxacin Solution
Product Images NDC 68180-421

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 68180-421). 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 (29272b83 77cf 4cd1 9aed B80d0cc6edb5 01)

Chemical structure of moxifloxacin hydrochloride, showing its molecular formula C21H24FN3O4·HCl and molecular weight of 437.9 g/mol. The diagram illustrates the arrangement of atoms and bonds in the molecule.*

FDA Label Image

Image (42db7e00 43ec 4fa6 9405 68cbcca5f79c 154 1)

MOXIFLOXACIN ophthalmic solution 5 mg/mL, shown in a white plastic dropper bottle with black text and design elements. The label includes the proprietary name MOXIFLOXACIN and the dosage strength, with the labeler Lupin Pharmaceuticals, Inc. indicated as the manufacturer.*

FDA Label Image

Container (29272b83 77cf 4cd1 9aed B80d0cc6edb5 02)

Label for MOXIFLOXACIN Ophthalmic Solution USP 0.5% (5 mg/mL) in 3 mL size. The label indicates the product is for ophthalmic use, administered twice daily, and is manufactured by Lupin Limited, India. It includes barcodes, an area for batch and expiry overprinting, and states 'FOR USE IN THE EYES ONLY.'*

FDA Label Image

Carton (29272b83 77cf 4cd1 9aed B80d0cc6edb5 03)

Packaging label for Moxifloxacin Ophthalmic Solution USP 0.5%, a 3 mL solution for ophthalmic use by Lupin Pharmaceuticals, Inc. Label highlights twice daily dosage, Rx only, and usage for eyes only. Includes active ingredient concentration, usage instructions, storage conditions, and manufacturer details.*

* 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.