Home › NDC Lookup › RxCUI directory › RxCUI 1999021

Brimonidine tartrate 0.25 MG/ML Ophthalmic Solution [Lumify] — RxCUI 1999021

RxNorm drug concept · Semantic branded drug
RxCUI 1999021 Semantic branded drug · SBD ● Current RxNorm concept 2 FDA products 11 package NDCs Snapshot Jul 14, 2026

This page is curated, coded, and maintained by

Compiled from public NLM RxNorm and FDA (openFDA NDC directory) data sources. Editorial policy

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI1999021
Official nameBrimonidine tartrate 0.25 MG/ML Ophthalmic Solution [Lumify]
Concept typeSemantic branded drug (SBD)
RxNorm statusCurrent RxNorm concept
Also known asLumify 0.025 % Ophthalmic Solution; Lumify 0.25 MG/ML Ophthalmic Solution
FDA products mapped2
Package NDCs mapped11
Reported Medicaid activity (SDUD)410 prescriptions · 4 state & territory Medicaid programs · latest period Q4 2025
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Brimonidine Ophthalmic: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • Brimonidine eye drops are used to lower the pressure inside your eye — what doctors call intraocular pressure. High eye pressure is a key risk factor for glaucoma-related vision da...
  • What exactly is brimonidine eye drops used for?
  • The usual routine is one drop in the affected eye or eyes, three times a day — roughly 8 hours apart, so think morning, afternoon, and evening. If you use other eye drops too, wait...
  • The most common ones are eye redness, itching, a burning or stinging sensation, and dry mouth. Some people also notice drowsiness or blurred vision. These are usually manageable, b...
📖 Read our full Brimonidine Ophthalmic guide →

🕸️ Concept Web — How Brimonidine tartrate 0.25 MG/ML Ophthalmic Solut... Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept Brimonidine tartrate 0.25 MG/ML Ophthalmic Solution [Lumify] RxCUI 1999021

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 2

    The active substance itself — no strength, form, or brand attached yet.

    • Brimonidine 134615
    • Brimonidine tartrate 39171
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Lumify 1999017
  3. Dose forms 9

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Brimonidine Ophthalmic Solution 378723
    • Brimonidine tartrate Ophthalmic Solution 2645974
    • Brimonidine Ophthalmic Product 1163094
    • Brimonidine tartrate Ophthalmic Product 2660235
    • Brimonidine Ophthalmic Solution [Lumify] 1999019
    • Brimonidine tartrate Ophthalmic Solution [Lumify] 2658921
    • Lumify Ophthalmic Product 1999020
    • Ophthalmic Solution 7670
    • +1 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 14 of 15 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Brimonidine tartrate 0.25 MG/ML Ophthalmic Solution SCD · 1999016
  • Brimonidine tartrate 0.25 MG/ML SCDC · 1999015
  • Brimonidine Ophthalmic Solution SCDF · 378723
  • Brimonidine tartrate Ophthalmic Solution SCDFP · 2645974
  • Brimonidine Ophthalmic Product SCDG · 1163094
  • Brimonidine tartrate Ophthalmic Product SCDGP · 2660235

Brand-Name Concepts

  • Brimonidine tartrate 0.25 MG/ML [Lumify] SBDC · 1999018
  • Brimonidine Ophthalmic Solution [Lumify] SBDF · 1999019
  • Brimonidine tartrate Ophthalmic Solution [Lumify] SBDFP · 2658921
  • Lumify Ophthalmic Product SBDG · 1999020
  • Lumify BN · 1999017

📦 FDA Products & Package NDCs

2 products · 11 package NDCs
11 package NDCs map to RxCUI 1999021 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
24208-0537-01 1 AMPULE in 1 CARTON (24208-537-01) / .4 mL in 1 AMPULE LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2019-05-01
24208-0537-05 1 BOTTLE, DROPPER in 1 CARTON (24208-537-05) / 5 mL in 1 BO... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2020-09-25
24208-0537-08 1 BOTTLE, DROPPER in 1 CARTON (24208-537-08) / 2.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2017-12-22
24208-0537-10 1 AMPULE in 1 CARTON (24208-537-10) / .4 mL in 1 AMPULE LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2019-05-01
24208-0537-15 2 BOTTLE, DROPPER in 1 CARTON (24208-537-15) / 7.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2019-04-30
24208-0537-25 1 BOTTLE, DROPPER in 1 CARTON (24208-537-25) / 7.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2017-12-22
24208-0537-35 1 BOTTLE, DROPPER in 1 CARTON (24208-537-35) / 3.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2023-05-02
24208-0537-75 1 BOTTLE, DROPPER in 1 CARTON (24208-537-75) / 7.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2017-12-22
24208-0537-99 1 BOTTLE, DROPPER in 1 CARTON (24208-537-99) / 2.5 mL in 1... LUMIFY Redness Reliever Eye Drops Bausch & Lomb Incorporated 2017-12-22
24208-0538-05 5 AMPULE in 1 POUCH (24208-538-05) / .4 mL in 1 AMPULE LUMIFY PRESERVATIVE FREE EYE DROPS Bausch & Lomb Incorporated 2025-01-01
24208-0538-20 4 POUCH in 1 CARTON (24208-538-20) / 5 AMPULE in 1 POUCH /... LUMIFY PRESERVATIVE FREE EYE DROPS Bausch & Lomb Incorporated 2025-01-01
Observed labelers: Bausch & Lomb Incorporated (11) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

💲 Pricing (NADAC)

NADAC is CMS's National Average Drug Acquisition Cost — roughly what pharmacies pay to buy the drug. It is an acquisition benchmark, not your copay.
Per ml · median
$2.7267
Range $1.9991–$3.4544 · middle 50% $2.3629–$3.0906 · 2 NDCs
Latest compatible distributions from the CMS NADAC file · dataset watermark 2026-07-10. Prices vary by package and pharmacy; a distribution is shown instead of one misleading number. Rows the dataset is silent on carry no price. No zero-cost conclusion should be drawn.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.