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- NSN 6505-01-517-1139
6505-01-517-1139
Description: Bimatoprost Ophthalmic Solution
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Export Restrictions
Any part(s) quoted or sold by MilSpec.parts and re-sold (to a third party) CANNOT be sold to a USA embargoed country, company, entity, or person(s). Depending on the ECCN, these commodities may require export license or exception. Diversion contrary to U.S. law is prohibited. Unless otherwise noted, this sale, order or quote may include Munitions List Items (MLI) or Commerce Controlled List Items (CCLI). MLI/CCLI property is controlled by the US Government and in many cases cannot be transferred (exported, sold or given) to a foreign country, a non-US Citizen/National or a non- Permanent US Resident without a valid State/Commerce Department export authorization. It is the responsibility of (the Purchaser) to determine what the applicable requirements may be, to obtain all necessary authorizations, licenses or approvals and are subject to both review and acceptance by MilSpec.parts. The use, disposition, export and re-export of the property covered or included in this sale, order or quote is subject to the provisions of law referenced in End-Use Certificate DLA form 1822, DEC 2001, including, but not limited to, the Arms Export Control Act (22 USC 2751 et seq.); Export Administration Act of 1979 (50 USC App. 2401 et seq.) as contained under Executive Order 12924; International Traffic in Arms Regulations (22 CFR 120 et seq.); Export Administration Regulations (15 CFR 730 et seq.); Foreign Assets Control Regulations (31 CFR 500 et seq.) and the Espionage Act (18 USC 793 et seq.)
6505-01-517-1139 Properties
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NSN:6505-01-517-1139
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Description:Bimatoprost Ophthalmic Solution
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Shelf Life:N/A
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DEMIL:NO
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UOM:--
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Part Name Assigned By Controlling Agency:Lumigan, bimatoprost ophthalmic solution, 0.03 pct
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Special Features:Does not require refrigeration; available in 2.5 ml and 5 ml sizes; has been reported to cause changes to pigmented tissues; including increased pigmentation and growth of eyelashes and increased pigmentation of the iris and periorbital tissue, eyelid, changes may be permanent
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Functional Description:Is indicated for the reduction of elevated intraocular pressure, iop, in patients with open-angle glaucoma or ocular hypertension who are intolerant of other iop-lowering medications or insufficiently responsive to another iop lowering medication; provides powerful iop reduction that remains consistent over time, both in number of patients achieving low target pressure and percentage reduction