NDC codes

FDA NDC Directory
Product NDC (as listed)51672-1267Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51672-1267Add 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
51672-1267-551672126705516721267051 TUBE in 1 CARTON (51672-1267-5) / 5 g in 1 TUBEMarketed from Oct 1, 1986
51672-1267-851672126708516721267081 TUBE in 1 CARTON (51672-1267-8) / 7.5 g in 1 TUBEMarketed from Oct 1, 1986

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
Sun Pharmaceutical Industries, Inc.NDC labeler code 51672
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 070730
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 51672-1267_3ed69275-ac41-bd44-e063-6394a90ad36aSPL ID 3ed69275-ac41-bd44-e063-6394a90ad36aSPL set ID b353c8b1-9088-4969-8199-37876f2461ccRxCUI 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

N451672126705 followed by a unit qualifier and the quantity

Package 51672-1267-05. 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)

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 51672-1267

What is NDC 51672-1267?
51672-1267 is the product NDC for Triamcinolone Acetonide, Triamcinolone acetonide 1 mg/g paste, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 2 package NDCs, 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?
Sun Pharmaceutical Industries, Inc., NDC labeler code 51672. 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?
218 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 219 Triamcinolone Acetonide NDCs

Other NDCs under ANDA 070730

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

FDA NDC Directory listings under ANDA 070730
ProductStrengthForm · routeLabelerProduct NDC
Oralonetriamcinolone acetonideTriamcinolone acetonide 1 mg/gPasteDentalSun Pharmaceutical Industries, Inc.51672-1335
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gPasteDentalPreferred Pharmaceuticals Inc68788-7814

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