NDC 24208-537

LUMIFY Redness Reliever Eye Drops

Brimonidine Tartrate

LUMIFY Redness Reliever Eye Drops is a Ophthalmic Solution/ Drops in the Human Otc Drug category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is Brimonidine Tartrate.

Product ID24208-537_022de945-0b26-40ae-8e88-d3fe2464d106
NDC24208-537
Product TypeHuman Otc Drug
Proprietary NameLUMIFY Redness Reliever Eye Drops
Generic NameBrimonidine Tartrate
Dosage FormSolution/ Drops
Route of AdministrationOPHTHALMIC
Marketing Start Date2017-12-22
Marketing CategoryNDA / NDA
Application NumberNDA208144
Labeler NameBausch & Lomb Incorporated
Substance NameBRIMONIDINE TARTRATE
Active Ingredient Strength0 mg/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 24208-537-01

1 AMPULE in 1 CARTON (24208-537-01) > .4 mL in 1 AMPULE
Marketing Start Date2019-05-01
NDC Exclude FlagN
Sample Package?Y

NDC SPL Data Element Entries

NDC 24208-537-15 [24208053715]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-04-30

NDC 24208-537-08 [24208053708]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-12-22

NDC 24208-537-01 [24208053701]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-01

NDC 24208-537-25 [24208053725]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Billing UnitML
Marketing Start Date2017-12-22

NDC 24208-537-10 [24208053710]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-01

NDC 24208-537-75 [24208053775]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-22

NDC 24208-537-99 [24208053799]

LUMIFY Redness Reliever Eye Drops SOLUTION/ DROPS
Marketing CategoryNDA
Application NumberNDA208144
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-12-22

Drug Details

Active Ingredients

IngredientStrength
BRIMONIDINE TARTRATE.25 mg/mL

OpenFDA Data

SPL SET ID:022de945-0b26-40ae-8e88-d3fe2464d106
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1999021
  • 1999016
  • UPC Code
  • 0310119537251
  • NDC Crossover Matching brand name "LUMIFY Redness Reliever Eye Drops" or generic name "Brimonidine Tartrate"

    NDCBrand NameGeneric Name
    24208-537LUMIFY Redness Reliever Eye DropsBRIMONIDINE TARTRATE
    0023-9177ALPHAGAN Pbrimonidine tartrate
    0023-9321ALPHAGAN Pbrimonidine tartrate
    17478-715BrimonidineBrimonidine Tartrate
    50090-1046BrimonidineBrimonidine Tartrate
    14445-400Brimonidine TartrateBrimonidine Tartrate
    24208-411Brimonidine TartrateBrimonidine Tartrate
    25685-715Brimonidine Tartratebrimonidine tartrate
    42843-501Brimonidine TartrateBrimonidine Tartrate
    50090-1800Brimonidine TartrateBrimonidine Tartrate
    50090-4224Brimonidine TartrateBrimonidine Tartrate
    60505-0564Brimonidine Tartratebrimonidine tartrate
    61314-143Brimonidine TartrateBrimonidine Tartrate
    61314-144Brimonidine TartrateBrimonidine Tartrate
    63629-8792Brimonidine TartrateBrimonidine Tartrate
    0299-5980Mirvasobrimonidine tartrate

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