Brimonidine Tartrate Ophthalmic Solution, 0.15% Solution/ Drops
Product Images NDC 62332-661

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Brimonidine Tartrate Ophthalmic Solution, 0.15% (NDC 62332-661). 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

Brimonidine-bottle-10ml (Brimonidine Bottle 10ml)

Brimonidine-bottle-10ml (Brimonidine Bottle 10ml)
Label for Brimonidine Tartrate ophthalmic solution 0.15%, sterile eye drops, 10 mL, by Alembic Pharmaceuticals Inc. The label includes active ingredient, preservative, usual dosage instructions, storage conditions, manufacturing location, and product barcodes. The label states Rx only and shows NDC 62332-661-10.*
FDA Label Image

Brimonidine-bottle-15ml (Brimonidine Bottle 15ml)

Brimonidine-bottle-15ml (Brimonidine Bottle 15ml)
Label of Brimonidine Tartrate ophthalmic solution 0.15%, a sterile eye drop solution in a 15 mL container. The product is labeled Rx only and manufactured for Alembic Pharmaceuticals Inc. The label includes details on active ingredient concentration, preservative use, storage instructions, and has a barcode with the product NDC 62332-661-15.*
FDA Label Image

Brimonidine-bottle-5ml (Brimonidine Bottle 5ml)

Brimonidine-bottle-5ml (Brimonidine Bottle 5ml)
Label for Brimonidine Tartrate ophthalmic solution 0.15%, sterile eye drops in a 5 mL bottle. The label displays the active ingredient concentration, storage instructions, manufacturer Alembic Pharmaceuticals Inc., and includes a barcode. It indicates prescription use only and a manufacture date of March 2023.*
FDA Label Image

Brimonidine-carton-10ml (Brimonidine Carton 10ml)

Brimonidine-carton-10ml (Brimonidine Carton 10ml)
Packaging label for Brimonidine Tartrate ophthalmic solution 0.15%, sterile eye drops in a 10 mL container, manufactured by Alembic Pharmaceuticals Inc. Label includes NDC 62332-661-10, active ingredient concentration, sterility and prescription-only designation, and storage instructions. The label features an image of a human eye, barcode, batch coding, and manufacturing information.*
FDA Label Image

Brimonidine-carton-15ml (Brimonidine Carton 15ml)

Brimonidine-carton-15ml (Brimonidine Carton 15ml)
The packaging label for Brimonidine Tartrate Ophthalmic Solution 0.15% sterile drops, 15 mL, by Alembic Pharmaceuticals Inc. The label displays the active ingredient concentration, manufacturer details (Alembic Pharmaceuticals Limited, India), barcode, and storage instructions. It includes product usage information and a grayscale image of a human eye on the front panels.*
FDA Label Image

Brimonidine-carton-5ml (Brimonidine Carton 5ml)

Brimonidine-carton-5ml (Brimonidine Carton 5ml)
Packaging label for Brimonidine Tartrate Ophthalmic Solution 0.15%, sterile, 5 mL solution drops by Alembic Pharmaceuticals Inc. The label shows the active ingredient concentration 0.15%, product usage as Rx only, manufacturing details, and a grayscale eye illustration. It also lists inactive ingredients and storage instructions, with NDC 62332-661-05.*
FDA Label Image

Brimonidine-structure (Brimonidine Structure)

Brimonidine-structure (Brimonidine Structure)
Chemical structure diagram depicting Brimonidine Tartrate, the active ingredient in Brimonidine Tartrate ophthalmic solution 0.15%. The illustration shows the molecular components and bonding arrangements typical for this compound used in ophthalmic solutions.*

* 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.