Azelastine Hydrochloride Solution/ Drops
Product Images NDC 47335-938

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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)

Azelastine-label (Azelastine Label)
This is a medication container label for Azelastine Hydrochloride, containing Ophthalmic Solution at 0.05% concentration. It suggests storing the solution upright at 20-25°C or 68-77°F with excursions allowed at 5 to 30°C. The usual dosage is 1 drop per affected eye(s) twice daily. It was manufactured by Sun Pharmaceutical Ind. Ltd. for the Eye Only, and its batch number is not included in this label. The label also mentions a package insert for full prescribing information.*
FDA Label Image

Chemical Structure (Azelastine Str)

FDA Label Image

Spl-azelastine-carton (Spl Azelastine Carton)

Spl-azelastine-carton (Spl Azelastine Carton)
This text is a description of a medication called Azelastine Hydrochloride Ophthalmic Solution. The solution is intended for use in the eyes only and comes in a 6 mL bottle. Each mL contains 0.5 mg of azelasting hydrochloride, among other substances. The package insert should be consulted for full prescribing information. The usual dosage is 1 drop twice daily in each affected eye. The medication should be stored upright at a temperature range of 20° to 25°C, with excursions permitted from 15° to 30°C. The medication is distributed by Sun Pharmaceutical Industries Inc., located in Cranbury, NJ. However, the medication is manufactured by Sun Pharmaceutical Industries Ltd., located in Halol-389 350, Gujarat, India. The packaging has an NDC number of 47335-938-90, and the medication is only available with a prescription (Rx only).*

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