Azelastine Hydrochloride Ophthalmic Solution 0.05% Solution/ Drops
Product Images NDC 62332-506

3 FDA label images from Alembic Pharmaceuticals Inc. · 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 Ophthalmic Solution 0.05% (NDC 62332-506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Azelastine-hydrochloride-str (Azelastine Hydrochloride Str)
Chemical structure diagram of Azelastine Hydrochloride, showing the molecular structure with labeled atoms and the hydrochloride component (HCl).*
FDA Label Image

Bottle Label

Bottle Label
Label of Azelastine Hydrochloride Ophthalmic Solution 0.05% drops, 6 mL, for ophthalmic use. The label includes the NDC 62332-506-06 and specifies the active ingredient concentration as 0.05%. The label also notes it is for Rx only, storage instructions, and manufacturers Alembic Pharmaceuticals Inc., Bedford, NJ, USA, with the product made in India.*
FDA Label Image

Carton Label

Carton Label
Packaging label for Azelastine Hydrochloride Ophthalmic Solution USP 0.05%, a sterile ophthalmic solution in a 6 mL bottle. The label includes the NDC 62332-506-06 and notes the product is Rx only and for use in the eyes only. Manufactured by Gland Pharma Limited, India, and labeled by Alembic Pharmaceuticals Inc., Bedminster, NJ. Additional details include storage instructions and ingredient listing.*

* 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.