NDC codes

FDA NDC Directory
Product NDC (as listed)71921-185Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71921-0185Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71921-185-0571921018505719210185055 mg in 1 BOTTLE, PLASTIC (71921-185-05)Marketed from Jan 15, 2022
71921-185-10719210185107192101851010 mg in 1 BOTTLE, PLASTIC (71921-185-10)Marketed from Jan 15, 2022
71921-185-15719210185157192101851515 mg in 1 BOTTLE, PLASTIC (71921-185-15)Marketed from Jan 15, 2022

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Brimonidine Tartrate
Generic name (nonproprietary)
brimonidine tartrate
Active ingredients
Brimonidine tartrate — 2 mg/mg
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Florida Pharmaceutical Products, LLCNDC labeler code 71921
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 091691
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 71921-185_81960280-6045-44e8-a499-6f737a92c7f2SPL ID 81960280-6045-44e8-a499-6f737a92c7f2SPL set ID a25f7abf-e066-4d16-a0ba-6150bdace81dRxCUI 861200UNII 4S9CL2DY2H
Pharmacologic class
alpha-Adrenergic Agonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471921018505 followed by a unit qualifier and the quantity

Package 71921-0185-05. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Brimonidine tartrate ophthalmic solution, 0.2% is indicated for lowering intraocular pressure in patients with open-angle glaucoma or ocular hypertension. The IOP lowering efficacy of Brimonidine tartrate ophthalmic solution, 0.2% diminishes over time in some patients. This loss of effect appears with a variable time of onset in each patient and should be closely monitored. Brimonidine Tartrate Ophthalmic Solution, 0.2% is an alpha adrenergic agonist indicated for lowering intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71921-185

What is NDC 71921-185?
71921-185 is the product NDC for Brimonidine Tartrate, Brimonidine tartrate 2 mg/mg solution/ drops, listed with the FDA by Florida Pharmaceutical Products, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Brimonidine Tartrate.
What is the active ingredient?
Brimonidine tartrate.
Who is the labeler?
Florida Pharmaceutical Products, LLC, NDC labeler code 71921. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Brimonidine Tartrate?
21 other product NDCs are listed under this name. See all Brimonidine Tartrate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Brimonidine Tartrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicUpsher-Smith Laboratories, LLC0832-143500832-1435-0500832-1435-1000832-1435-15
brimonidine tartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicMicro Labs Limited42571-46242571-0462-5642571-0462-92
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicGland Pharma Limited68083-62668083-0626-0568083-0626-1068083-0626-15
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-56670069-0566-01
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-56770069-0567-01
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-56870069-0568-01
Brimonidine TartrateBrimonidine tartrate 1.5 mg/mLSolution/ dropsOphthalmicUpsher-Smith Laboratories, LLC0832-142000832-1420-0500832-1420-1000832-1420-15
Brimonidine tartrateBrimonidine tartrate 2 mg/mLSolution/ dropsOphthalmicMicro Labs Limited42571-41942571-0419-5642571-0419-5742571-0419-92
Brimonidine tartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicPacific Pharma, Inc.82182-32182182-0321-0582182-0321-1082182-0321-15
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicApotex Corp.60505-057760505-0577-0160505-0577-0260505-0577-03

All 22 Brimonidine Tartrate NDCs

Other NDCs under ANDA 091691

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 091691
ProductStrengthForm · routeLabelerProduct NDC
Brimonidine TartrateBrimonidine tartrate 2 mg/mgSolution/ dropsOphthalmicIndoco Remedies Limited14445-400

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