Azelastine Hydrochloride Solution/ Drops
Product Images NDC 46708-506

View Photos of 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 Azelastine Hydrochloride (NDC 46708-506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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-hydrochloride-str (Azelastine Hydrochloride Str)

Azelastine-hydrochloride-str (Azelastine Hydrochloride Str)
Chemical structure of azelastine hydrochloride, showing its molecular arrangement including ring structures and chlorine and hydrochloride groups.*
FDA Label Image

Bottle-label-alembic-dm (Bottle Label Alembic Dm)

Bottle-label-alembic-dm (Bottle Label Alembic Dm)
The label for Azelastine Hydrochloride Ophthalmic Solution, USP 0.05% shows a 6 mL bottle. It is an ophthalmic solution containing 0.5 mg/mL azelastine hydrochloride. The label indicates storage instructions, usage directions for the eyes, and manufacturing by Alembic Pharmaceuticals Limited in India. It also includes the NDC 46708-506-06 and barcode.*
FDA Label Image

Carton-label-alembic-dm (Carton Label Alembic Dm)

Carton-label-alembic-dm (Carton Label Alembic Dm)
The label for Azelastine Hydrochloride Ophthalmic Solution USP 0.05% shows a 6 mL ophthalmic solution for prescription use. The packaging is by Alembic Pharmaceuticals Limited, with storage instructions and usual dosage for eye drops. The label includes an image of an eye, the product strength, and batch coding information on the top flap.*

* 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.