What is NDC 59088-730?

59088-730 is the product NDC for Triasil (triamcinolone acetonide) kit, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Triasil (Triamcinolone Acetonide).

PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Triasil?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Triasil NDC 59088-730 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59088-730Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59088-0730Add 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
59088-730-00	5908807300059088073000	1 KIT in 1 KIT (59088-730-00) * 1 TUBE in 1 CARTON (45802-055-36) / 80 g in 1 TUBEMarketed from Jan 20, 2023

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): Triasil
Generic name (nonproprietary): triamcinolone acetonide
Dosage form: Kit
Labeler: PureTek CorporationNDC labeler code 59088
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jan 20, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 59088-730_f3095546-7f72-2665-e053-2995a90aff07SPL ID f3095546-7f72-2665-e053-2995a90aff07SPL set ID dcf6c630-6f5d-3d2f-e053-2995a90ad812RxCUI 1085636UPC 0359088730003

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

N459088073000 followed by a unit qualifier and the quantity

Package 59088-0730-00. 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 Jan 24, 2023.

Indications (excerpt from the label)

INDICATIONS AND USAGE Topical corticosteroids are 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)

About NDC 59088-730

What is NDC 59088-730?: 59088-730 is the product NDC for Triasil (triamcinolone acetonide) kit, listed with the FDA by PureTek Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Triasil (Triamcinolone Acetonide).
Who is the labeler?: PureTek Corporation, NDC labeler code 59088. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triasil?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Triasil (Triamcinolone acetonide) NDC 59088-730