Olopatadine Hydrochloride Solution/ Drops
Product Images NDC 62332-502

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 Olopatadine Hydrochloride (NDC 62332-502). 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

Olopatadine-carton11 (Olopatadine Carton11)

Olopatadine-carton11 (Olopatadine Carton11)
Carton label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, 2.5 mL, by Alembic Pharmaceuticals Inc. Label includes dosage instructions, storage information, active ingredient concentration (2.22 mg/mL olopatadine hydrochloride equivalent to 2 mg olopatadine), preservative content, inactives, and warnings. The product is for prescription use in the eyes only and is manufactured by Gland Pharma Limited, India.*
FDA Label Image

Olopatadine-container (Olopatadine Container)

Olopatadine-container (Olopatadine Container)
Label for Olopatadine Hydrochloride Ophthalmic Solution USP 0.2%, 2.5 mL vial. The label states the solution is for use in the eyes only with a once daily dosage. It includes storage instructions, manufacturer Alembic Pharmaceuticals, Inc., and barcode with NDC 62332-502-03.*
FDA Label Image

Olopatadine-structure (Olopatadine Structure)

Olopatadine-structure (Olopatadine Structure)
Chemical structure diagram of olopatadine hydrochloride, the active ingredient in OLOPATADINE HYDROCHLORIDE 2 mg/mL ophthalmic solution/drops by Alembic Pharmaceuticals Inc.*

* 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.