Moxifloxacin Ophthalmic Solution Solution/ Drops
Product Images NDC 62332-505

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Ophthalmic Solution (NDC 62332-505). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic 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

Moxifloxacin-bottle1 (Moxifloxacin Bottle1)

Label for Moxifloxacin Ophthalmic Solution, USP 0.5% (5 mg/mL) in a 3 mL bottle, manufactured by Alembic Pharmaceuticals Inc. The label indicates the product is for topical ophthalmic use, contains moxifloxacin hydrochloride equivalent to 5 mg per mL, and provides storage instructions (2°C to 25°C). The label includes the NDC 62332-505-03, barcode, and manufacturer details with a lot and expiration date area.*

FDA Label Image

Moxifloxacin-carton (Moxifloxacin Carton)

Moxifloxacin ophthalmic solution USP 0.5% 3 mL carton packaging for topical eye use. The label displays the NDC number 62332-505-03 and active ingredient details: moxifloxacin hydrochloride 5.45 mg per mL equivalent to moxifloxacin 5 mg. The product is Rx only, manufactured for Alembic Pharmaceuticals, Inc., Bedminster, NJ, USA, and made by Gland Pharma Limited, Hyderabad, India. The packaging includes storage instructions and a barcode.*

FDA Label Image

Moxifloxacin-structure (Moxifloxacin Structure)

Chemical structure diagram of moxifloxacin hydrochloride, the active ingredient in Moxifloxacin ophthalmic solution 5 mg/mL by Alembic Pharmaceuticals Inc. The image shows the molecular formula C21H24FN3O4·HCl and molecular weight 437.9.*

* 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.