Azelastine Hydrochloride Solution/ Drops
Product Images NDC 61314-308

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Azelastine Hydrochloride (NDC 61314-308). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Structure (Image 01)

FDA Label Image

Carton (Image 02)

Carton (Image 02)
NDC 61314-308-02 is a prescription ophthalmic solution for topical application in the eye. Each ml contains 0.5 mg of azelastine hydrochloride and 0.125 mg of benzalkonium chloride as the preservative. It is manufactured by Aon Laboratories, Inc., Fort Worth, Texas, for Grand Ophthalmic. It is stored upright between 2°C and 25°C, and usual dosage is one drop per affected eye twice daily as per prescribing information. The solution is sterile and packaged in a resistant wrapping. Keep out of reach of children.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.