NDC codes

FDA NDC Directory
Product NDC (as listed)0469-2760Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00469-2760Add 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
0469-2760-28004692760284 CARTON in 1 TRAY (0469-2760-28) / 1 BLISTER PACK in 1 CARTON (0469-2760-07) / 7 TABLET, FILM COATED in 1 BLISTER PACKMarketed from May 12, 2023 · Sample package

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Veozah
Generic name (nonproprietary)
fezolinetant
Active ingredients
Fezolinetant — 45 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 216578
Marketing start
Listing expires
Other FDA classes
Neurokinin 3 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0469-2760_462f0a23-98d6-4154-b113-322008069743SPL ID 462f0a23-98d6-4154-b113-322008069743SPL set ID cae9f798-24f9-4580-a4fc-e6c710cbda3cRxCUI 2637141, 2637147UNII 83VNE45KXX
Pharmacologic class
Neurokinin 3 Receptor Antagonist

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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400469276028 followed by a unit qualifier and the quantity

Package 00469-2760-28. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

VEOZAH ® is indicated for the treatment of moderate to severe vasomotor symptoms due to menopause. VEOZAH is a neurokinin 3 (NK3) receptor antagonist indicated for the treatment of moderate to severe vasomotor symptoms due to menopause. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 216578

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

FDA NDC Directory listings under NDA 216578
ProductStrengthForm · routeLabelerProduct NDC
VeozahfezolinetantFezolinetant 45 mg/1Tablet, Film coatedOralAstellas Pharma US, Inc.0469-2460
VeozahfezolinetantFezolinetant 45 mg/1Tablet, Film coatedOralAstellas Pharma US, Inc.0469-2660

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in