NDC codes

FDA NDC Directory
Product NDC (as listed)68071-3666Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-3666Add 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
68071-3666-3680713666031 TUBE in 1 CARTON (68071-3666-3) / 30 g in 1 TUBEMarketed from Aug 19, 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 acetonide1 mg/g
Dosage form
Cream
Route
Topical
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208848
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 68071-3666_200bed0d-df4c-7be8-e063-6294a90aa2d6SPL ID 200bed0d-df4c-7be8-e063-6294a90aa2d6SPL set ID 200bb913-a6ac-5a6b-e063-6294a90a161aRxCUI 1014314UNII F446C597KAUPC 0368071366631
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

N468071366603 followed by a unit qualifier and the quantity

Package 68071-3666-03. 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 .

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 208848

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

FDA NDC Directory listings under ANDA 208848
ProductStrengthForm · routeLabelerProduct NDC
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalDirect_rx72189-670
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalProficient Rx LP82804-145
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalREMEDYREPACK INC.70518-4527
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalEncube Ethicals, Inc.21922-062
Triamcinolone AcetonideTriamcinolone acetonide 1 mg/gCreamTopicalPreferred Pharmaceuticals Inc.68788-8753
triamcinolone acetonideTriamcinolone acetonide 1 mg/gCreamTopicalNuCare Pharmaceuticals,Inc.68071-4391

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