NDC codes

FDA NDC Directory
Product NDC (as listed)70069-566Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70069-0566Add 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
70069-566-0170069056601700690566011 BOTTLE in 1 CARTON (70069-566-01) / 5 mL in 1 BOTTLEMarketed from Aug 26, 2024

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 — 1 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 216906
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)
Identifiers
Product ID 70069-566_5a808f88-afeb-4ab3-b005-56b68b27dc7fSPL ID 5a808f88-afeb-4ab3-b005-56b68b27dc7fSPL set ID b8e108b3-aca8-4e3e-8577-37ac796148c3RxCUI 861204UNII 4S9CL2DY2HUPC 0370069566015, 0370069568019, 0370069567012
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

N470069056601 followed by a unit qualifier and the quantity

Package 70069-0566-01. 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 0.1% is an alpha-adrenergic receptor agonist indicated for the reduction of elevated intraocular pressure (IOP) in patients with open- angle glaucoma or ocular hypertension. Brimonidine tartrate ophthalmic solution is an alpha adrenergic receptor agonist indicated for the reduction of elevated 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 70069-566

What is NDC 70069-566?
70069-566 is the product NDC for Brimonidine Tartrate, Brimonidine tartrate 1 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, LLC70069-56770069-0567-01
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
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicAlembic Pharmaceuticals Limited46708-74946708-0749-0546708-0749-1046708-0749-15

All 22 Brimonidine Tartrate NDCs

Other NDCs under ANDA 216906

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

FDA NDC Directory listings under ANDA 216906
ProductStrengthForm · routeLabelerProduct NDC
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-567
Brimonidine TartrateBrimonidine tartrate 1 mg/mLSolution/ dropsOphthalmicSomerset Therapeutics, LLC70069-568

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