Triamcinolone Acetonide NDC 68071-2736

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2736Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2736Add 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 NDC	11-digit (billing)	Package	Copy
68071-2736-3	68071273603	1 TUBE in 1 CARTON (68071-2736-3) / 30 g in 1 TUBEMarketed from May 26, 2022

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: Cream
Route: Topical
Labeler: NuCare Pharmaceuticals,Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 040039
Marketing start: Nov 26, 1997
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 68071-2736_2a070c8c-180b-7288-e063-6294a90a6971SPL ID 2a070c8c-180b-7288-e063-6294a90a6971SPL set ID dff0403f-1c0c-3333-e053-2a95a90a4c09RxCUI 1014314UNII F446C597KAUPC 0368071273632
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N468071273603 followed by a unit qualifier and the quantity

Package 68071-2736-03. 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 Dec 24, 2024.

Indications (excerpt from the label)

INDICATIONS AND USAGE Triamcinolone acetonide cream, 0.1% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid-responsive dermatoses.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 040039

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

FDA NDC Directory listings under ANDA 040039
Product	Strength	Form · route	Labeler	Product NDC
Triamcinolone Acetonide	Triamcinolone acetonide 1 mg/g	CreamTopical	Sun Pharmaceutical Industries, Inc.	51672-1282
Triamcinolone Acetonide	Triamcinolone acetonide 1 mg/g	CreamTopical	Preferred Pharmaceuticals Inc.	68788-8356
Triamcinolone Acetonide	Triamcinolone acetonide 1 mg/g	CreamTopical	Proficient Rx LP	82804-071