NDC codes

FDA NDC Directory
Product NDC (as listed)82667-800Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82667-0800Add 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
82667-800-0182667080001826670800011 BLISTER PACK in 1 CARTON (82667-800-01) / 1 VIAL, GLASS in 1 BLISTER PACK / 1 mL in 1 VIAL, GLASSMarketed from Oct 1, 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)
Triesence
Generic name (nonproprietary)
triamcinolone acetonide
Active ingredients
Triamcinolone acetonide — 40 mg/mL
Dosage form
Injection, Suspension
Route
Ophthalmic
Labeler
Harrow Eye, LLCNDC labeler code 82667
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 022048
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 82667-800_5386eec5-c123-04b8-e063-6294a90a2952SPL ID 5386eec5-c123-04b8-e063-6294a90a2952SPL set ID 2267978c-72ad-9229-e063-6394a90a09d0RxCUI 1086259, 1792144UNII F446C597KA
Pharmacologic class
Corticosteroid

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

N482667080001 followed by a unit qualifier and the quantity

Package 82667-0800-01. 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)

TRIESENCE suspension is a synthetic corticosteroid indicated for: • Treatment of the following ophthalmic diseases: sympathetic ophthalmia, temporal arteritis, uveitis, and ocular inflammatory conditions unresponsive to topical corticosteroids. ( 1.1 ) • Visualization during vitrectomy. ( 1.2 ) 1.1 Ophthalmic Diseases TRIESENCE (triamcinolone acetonide injectable suspension) 40 mg/mL is indicated for: • sympathetic ophthalmia, • temporal arteritis, • uveitis, and • ocular inflammatory conditions unresponsive to topical corticosteroids. 1.2 Visualization During Vitrectomy TRIESENCE suspension is indicated for visualization during vitrectomy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82667-800

What is NDC 82667-800?
82667-800 is the product NDC for Triesence (triamcinolone acetonide), Triamcinolone acetonide 40 mg/mL injection, suspension, listed with the FDA by Harrow Eye, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Triesence (Triamcinolone acetonide).
What is the active ingredient?
Triamcinolone acetonide.
Who is the labeler?
Harrow Eye, LLC, NDC labeler code 82667. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triesence?
1 other product NDC are listed under this name. See all Triesence 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 Triesence NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Triesencetriamcinolone acetonideTriamcinolone acetonide 40 mg/mLInjection, SuspensionOphthalmicNovartis Pharmaceuticals Corporation0078-089700078-0897-78

Other NDCs under NDA 022048

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

FDA NDC Directory listings under NDA 022048
ProductStrengthForm · routeLabelerProduct NDC
Triesencetriamcinolone acetonideTriamcinolone acetonide 40 mg/mLInjection, SuspensionOphthalmicNovartis Pharmaceuticals Corporation0078-0897

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