NDC codes

FDA NDC Directory
Product NDC (as listed)70069-232Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70069-0232Add 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
70069-232-0170069023201700690232011 BOTTLE in 1 CARTON (70069-232-01) / 10 mL in 1 BOTTLEMarketed from Mar 11, 2019

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/mL
Dosage form
Solution/ drops
Route
Ophthalmic
Labeler
Somerset Therapeutics, LLCNDC labeler code 70069
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208992
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 70069-232_fd76c55c-cb68-4884-8a1a-a4c6bf66562aSPL ID fd76c55c-cb68-4884-8a1a-a4c6bf66562aSPL set ID cdb8620f-adfa-4433-b285-9c42334f8600RxCUI 861200UNII 4S9CL2DY2HUPC 0370069231012, 0370069232019, 0370069233016
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

N470069023201 followed by a unit qualifier and the quantity

Package 70069-0232-01. 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 an alpha adrenergic agonist indicated for lowering intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. Brimonidine tartrate ophthalmic solution 0.2% is indicated for lowering intraocular pressure (IOP) in patients with open-angle glaucoma or ocular hypertension. The IOP lowering efficacy of brimonidine tartrate ophthalmic solution 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.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70069-232

What is NDC 70069-232?
70069-232 is the product NDC for Brimonidine Tartrate, Brimonidine tartrate 2 mg/mL solution/ drops, listed with the FDA by Somerset Therapeutics, LLC. It has 1 package NDC, 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?
Somerset Therapeutics, LLC, NDC labeler code 70069. 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 208992

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

FDA NDC Directory listings under ANDA 208992
ProductStrengthForm · routeLabelerProduct NDC
Brimonidine TartrateBrimonidine tartrate 2 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-231
Brimonidine TartrateBrimonidine tartrate 2 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-233

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