Bimatoprost Solution/ Drops
Product Images NDC 65862-802

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bimatoprost (NDC 65862-802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (0.03%)

NDC 65862-802-44 is an ophthalmic solution called Atoprost manufactured by Aurobindo Pharma USA. The solution is meant for use in the eyes only and should be stored at 2° to 25°C (36° to 77°1). The package comes in a 2.5 mL bottle and requires a prescription.*

FDA Label Image

Package Label-principal Display Panel (0.03%)

This is a description of Bimatoprost Ophthalmic Solution 0.03%. It is for use in the eyes only and a prescription is required. The solution is sterile and comes in a 25ml bottle. The product is manufactured by Aurobindo and contains active ingredient bimatoprost 0.3% oyl and preservative benzalkonium chloride 0.5 g/. The product has an inactive ingredient list that includes acetic acid, monohydrate: Sodium hydrogen phosphate, Dihydrate; Sodium hydroxide and hydrochloric acid may be added to adjust pH. The usual dosage is 1 drop in the affected eye(s) once daily in the evening. This product should be stored at 2-25°C (36°- 77°F).*

FDA Label Image

Package Label-principal Display Panel (0.03%)

This text appears to be a label or package insert for an ophthalmic solution called Bimatoprost made by Aurobindo Pharma USA, Inc. The label indicates the storage temperature range, manufacturer information, drug code, and lot number. It also states that the solution is for use in the eyes only and requires a prescription. The text is not readable past the last word "i".*

FDA Label Image

Package Label-principal Display Panel (0.03%)

This is a description of Bimatoprost Ophthalmic Solution, a drug used to treat eye conditions. The solution is for use in the eyes only and requires a prescription. It comes in a sterile 2mL container with a usual dosage of one drop in the affected eye once daily in the evening. The solution contains bimatoprost, a preservative known as benzalkonium chloride, and other inactive ingredients. The pH level during shelf life ranges from 6.8 to 10.8. The package should be kept out of the reach of children, and it is not child-resistant. It is distributed by Aurobindo Pharma USA and has a manufacturer's code of TSDRUGS/ 1372010.*

FDA Label Image

Package Label-principal Display Panel (0.03%)

This is a drug label for Bimatoprost 0.03% Ophthalmic Solution manufactured in India for Aurobindo Pharma USA, Inc. The label contains information on storage temperature and the drug's National Drug Code (NDC) number. The drug is used for the eyes only and the label specifies prescription-only use. There is also a lot number and expiration date listed.*

FDA Label Image

Package Label-principal Display Panel (0.03%)

FDA Label Image

Chemical Structure (Bimatoprost Str)

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