Bimatoprost Solution/ Drops
Product Images NDC 60219-2149

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 Bimatoprost (NDC 60219-2149). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny Llc, 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

1 (Bimatoprost Ophthalmic Solution 1)

1 (Bimatoprost Ophthalmic Solution 1)
Chemical structure diagram of the active ingredient Bimatoprost, showing its molecular framework with functional groups and stereochemistry.*
FDA Label Image

001 (Bimatoprost Ophthalmic Solution 2)

001 (Bimatoprost Ophthalmic Solution 2)
Label for Bimatoprost Ophthalmic Solution 0.01%, sterile, 2.5 mL bottle. The label displays active ingredient Bimatoprost 0.1 mg per mL, preservative Benzalkonium chloride 0.15 mg, and storage instructions. It is distributed by Amneal Pharmaceuticals LLC and made in India, with a barcode and NDC 60219-2149-1.*
FDA Label Image

002 (Bimatoprost Ophthalmic Solution 3)

002 (Bimatoprost Ophthalmic Solution 3)
Packaging label for Bimatoprost Ophthalmic Solution 0.01%, 2.5 mL, by Amneal Pharmaceuticals NY LLC. The label highlights the active ingredient Bimatoprost at 0.1 mg per mL, with preservative benzalkonium chloride. It is indicated for eye use only, sterile, and labeled Rx only. The label includes manufacturer and distributor information, barcodes, and storage instructions.*
FDA Label Image

003 (Bimatoprost Ophthalmic Solution 4)

003 (Bimatoprost Ophthalmic Solution 4)
Label for Bimatoprost Ophthalmic Solution 0.01% (0.1 mg/mL) in a 5 mL bottle. The label includes active ingredient, preservative benzalkonium chloride 0.15 mg, and storage instructions. Distributed by Amneal Pharmaceuticals LLC, made in India. It is marked Rx only and sterile, with barcode and lot/expiration info areas indicated.*
FDA Label Image

004 (Bimatoprost Ophthalmic Solution 5)

004 (Bimatoprost Ophthalmic Solution 5)
Carton packaging label for Bimatoprost Ophthalmic Solution 0.01%, an eye drop solution in a 5 mL sterile bottle. The label includes the active ingredient concentration (0.1 mg per mL), preservatives, inactive ingredients, and storage instructions. It is labeled for Rx use only and manufactured by Amneal Pharmaceuticals NY LLC. The design features the Amneal logo and barcode.*
FDA Label Image

005 (Bimatoprost Ophthalmic Solution 6)

005 (Bimatoprost Ophthalmic Solution 6)
Label for Bimatoprost Ophthalmic Solution 0.01% (0.1 mg/mL) in a 7.5 mL container. The label includes active ingredient details, preservative (benzalkonium chloride), dosage instructions, storage conditions, and distributor information for Amneal Pharmaceuticals LLC. The label also displays the NDC 60219-2149 and barcode.*
FDA Label Image

006 (Bimatoprost Ophthalmic Solution 7)

006 (Bimatoprost Ophthalmic Solution 7)
Packaging label for Bimatoprost Ophthalmic Solution 0.01%, sterile liquid ophthalmic drops in a 7.5 mL bottle. Label shows the active ingredient concentration of 0.1 mg/mL, preservatives, and inactives. The product is Rx only and for eye use only. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. in India and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ.*

* 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.