Azelastine Hydrochloride Solution/ Drops
Product Images NDC 47335-938

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Azelastine Hydrochloride (NDC 47335-938). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Azelastine-label (Azelastine Label)

Label of Azelastine Hydrochloride Ophthalmic Solution 0.05%, a 6 mL sterile intraocular solution. It is for eye use only and available by prescription. The label includes storage instructions, manufacturer Sun Pharmaceutical Industries, Inc. (Gujarat, India), and dosage direction: 1 drop per affected eye twice daily.*

FDA Label Image

Chemical Structure (Azelastine Str)

Chemical structure of Azelastine Hydrochloride, showing its molecular framework with chlorine substitution and a hydrochloride group.*

FDA Label Image

Spl-azelastine-carton (Spl Azelastine Carton)

Packaging label for Azelastine Hydrochloride Ophthalmic Solution 0.05%, a 6 mL sterile intraocular solution by Sun Pharmaceutical Industries, Inc. The label includes dosage instructions, storage conditions, and manufacturer information. The product is for eye use only and prescription only. The NDC number 47335-938-90 is displayed with a barcode and Sun Pharma logo.*

* 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.