NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2318Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2318Add 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
72162-2318-2721622318021 TUBE in 1 CARTON (72162-2318-2) / 5 g in 1 TUBEMarketed from May 20, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Triamcinolone Acetonide
Generic name (nonproprietary)
triamcinolone acetonide
Active ingredients
Triamcinolone acetonide — 1 mg/g
Dosage form
Paste
Route
Dental
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214582
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 72162-2318_c0e105a9-5bbb-42e8-a00d-03bc260b6b95SPL ID c0e105a9-5bbb-42e8-a00d-03bc260b6b95SPL set ID c2b12aa8-1875-489b-8d16-fb588ad3cf54RxCUI 1085728UNII 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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N472162231802 followed by a unit qualifier and the quantity

Package 72162-2318-02. 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)

INDICATIONS AND USAGE Triamcinolone Acetonide Dental Paste USP, 0.1% is indicated for adjunctive treatment and for the temporary relief of symptoms associated with oral inflammatory lesions and ulcerative lesions resulting from trauma.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-2318

What is NDC 72162-2318?
72162-2318 is the product NDC for Triamcinolone Acetonide, Triamcinolone acetonide 1 mg/g paste, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Triamcinolone Acetonide.
What is the active ingredient?
Triamcinolone acetonide.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triamcinolone Acetonide?
220 other product NDCs are listed under this name. See all Triamcinolone Acetonide 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 Triamcinolone Acetonide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Triamcinolone AcetonideTriamcinolone acetonide 55 ug/1Spray, MeteredNasalAurohealth LLC58602-03558602-0035-0758602-0035-0858602-0035-09+1 more
Triamcinolone AcetonideTriamcinolone acetonide .25 mg/gCreamTopicalPreferred Pharmaceuticals Inc.68788-414868788-4148-01
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalDirect_rx72189-67072189-0670-30
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalDirect_Rx61919-23461919-0234-3061919-0234-80
Triamcinolone AcetonideTriamcinolone acetonide 400 mg/10mLInjection, SuspensionIntra-articular, IntramuscularREMEDYREPACK INC.70518-458270518-4582-00
Triamcinolone AcetonideTriamcinolone acetonide 40 mg/mLInjection, SuspensionIntra-articular, IntramuscularSagent Pharmaceuticals25021-05425021-0054-0125021-0054-0525021-0054-10
Triamcinolone acetonideTriamcinolone acetonide 5 mg/gOintmentTopicalREMEDYREPACK INC.70518-454670518-4546-00
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalREMEDYREPACK INC.70518-452770518-4527-00
Triamcinolone AcetonideTriamcinolone acetonide 55 ug/1Spray, MeteredNasalCARDINAL HEALTH 110, LLC. DBA LEADER 7000070000-074270000-0742-01
Triamcinolone AcetonideTriamcinolone acetonide 40 mg/mLInjection, SuspensionIntra-articular, IntramuscularDr. Reddy's Laboratories Inc43598-67743598-0677-1143598-0677-25

All 221 Triamcinolone Acetonide NDCs

Other NDCs under ANDA 214582

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

FDA NDC Directory listings under ANDA 214582
ProductStrengthForm · routeLabelerProduct NDC
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gPasteDentalQUAGEN PHARMACEUTICALS LLC70752-140

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