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Generated: November 13, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 208144

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NDA 208144 describes LUMIFY, which is a drug marketed by Bausch And Lomb Inc and is included in one NDA. It is available from one supplier. There is one patent protecting this drug. Additional details are available on the LUMIFY profile page.

The generic ingredient in LUMIFY is brimonidine tartrate. There are eleven drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the brimonidine tartrate profile page.
Summary for 208144
Tradename:LUMIFY
Applicant:Bausch And Lomb Inc
Ingredient:brimonidine tartrate
Patents:1
Medical Subject Heading (MeSH) Categories for 208144
Suppliers and Packaging for NDA: 208144
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LUMIFY brimonidine tartrate SOLUTION/DROPS;OPHTHALMIC 208144 NDA Bausch & Lomb Incorporated 24208-537 24208-537-08 1 BOTTLE, DROPPER in 1 CARTON (24208-537-08) > 2.5 mL in 1 BOTTLE, DROPPER
LUMIFY brimonidine tartrate SOLUTION/DROPS;OPHTHALMIC 208144 NDA Bausch & Lomb Incorporated 24208-537 24208-537-25 1 BOTTLE, DROPPER in 1 CARTON (24208-537-25) > 7.5 mL in 1 BOTTLE, DROPPER

Profile for product number 001

Active Rx/OTC/Discontinued:OTCDosage:SOLUTION/DROPS;OPHTHALMICStrength0.025%
Approval Date:Dec 22, 2017TE:RLD:Yes
Regulatory Exclusivity Expiration:Dec 22, 2020
Regulatory Exclusivity Use:NEW PRODUCT
Patent:➤ Try a Free TrialPatent Expiration:Jul 14, 2030Product Flag?Substance Flag?Delist Request?
Patented Use:RELIEVES REDNESS OF THE EYE DUE TO MINOR EYE IRRITATIONS

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