What is NDC 24338-150?

24338-150 is the product NDC for Triptodur (triptorelin) kit, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Azurity Pharmaceuticals, Inc., NDC labeler code 24338. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Triptodur?

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.

Triptodur NDC 24338-150 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)24338-150Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24338-0150Add 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
24338-150-20	2433801502024338015020	1 KIT in 1 CARTON (24338-150-20) * 2 mL in 1 VIAL * 2 mL in 1 SYRINGE, GLASSMarketed from Sep 8, 2017

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): Triptodur
Generic name (nonproprietary): triptorelin
Dosage form: Kit
Labeler: Azurity Pharmaceuticals, Inc.NDC labeler code 24338
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 208956
Marketing start: Sep 8, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 24338-150_1c06d8b5-edbc-4de7-a423-7588069d3c38SPL ID 1c06d8b5-edbc-4de7-a423-7588069d3c38SPL set ID f41380e7-b830-432d-a5f5-a872932f107eRxCUI 905053, 1944389

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

N424338015020 followed by a unit qualifier and the quantity

Package 24338-0150-20. 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 Sep 14, 2025.

Indications (excerpt from the label)

TRIPTODUR is indicated for the treatment of pediatric patients 2 years of age and older with central precocious puberty (CPP). TRIPTODUR is a gonadotropin releasing hormone (GnRH) agonist indicated for the treatment of pediatric patients 2 years and older with central precocious puberty. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24338-150

What is NDC 24338-150?: 24338-150 is the product NDC for Triptodur (triptorelin) kit, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Triptodur (Triptorelin).
Who is the labeler?: Azurity Pharmaceuticals, Inc., NDC labeler code 24338. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Triptodur?: 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.

Triptodur (Triptorelin) NDC 24338-150