What is NDC 72189-609?

72189-609 is the product NDC for Rizatriptan Benzoate ODT, Rizatriptan benzoate 10 mg/1 tablet, orally disintegrating, listed with the FDA by Direct_rx. It has 1 package NDC, shown above in 10- and 11-digit form.

Direct_rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Rizatriptan Benzoate ODT?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Rizatriptan Benzoate ODT NDC 72189-609

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-609Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0609Add 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
72189-609-18	7218906091872189060918	18 TABLET, ORALLY DISINTEGRATING in 1 CARTON (72189-609-18)Marketed from Jan 20, 2025

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): Rizatriptan Benzoate ODT
Generic name (nonproprietary): rizatriptan benzoate odt
Active ingredients: Rizatriptan benzoate — 10 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: Direct_rxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203146
Marketing start: Jan 20, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 72189-609_4d3aab18-54e6-cb65-e063-6394a90a9b26SPL ID 4d3aab18-54e6-cb65-e063-6394a90a9b26SPL set ID 2c29e066-c018-22e7-e063-6294a90a035cRxCUI 312837UNII WR978S7QHH
Pharmacologic class: Serotonin-1b and Serotonin-1d Receptor Agonist

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

N472189060918 followed by a unit qualifier and the quantity

Package 72189-0609-18. 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 Mar 17, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Rizatriptan benzoate orally disintegrating tablets are indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years old. Limitations of Use • Rizatriptan benzoate orally disintegrating tablets should only be used where a clear diagnosis of migraine has been established. If a patient has no response for the first migraine attack treated with rizatriptan benzoate orally disintegrating tablets, the diagnosis of migraine should be reconsidered before rizatriptan benzoate tablets are administered to treat any subsequent attacks. • Rizatriptan benzoate orally disintegrating tablets are not indicated for use in the management of hemiplegic or …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-609

What is NDC 72189-609?: 72189-609 is the product NDC for Rizatriptan Benzoate ODT, Rizatriptan benzoate 10 mg/1 tablet, orally disintegrating, listed with the FDA by Direct_rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Rizatriptan Benzoate ODT.
What is the active ingredient?: Rizatriptan benzoate.
Who is the labeler?: Direct_rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Rizatriptan Benzoate ODT?: 1 other product NDC are listed under this name. See all Rizatriptan Benzoate ODT NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Rizatriptan Benzoate ODT NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Rizatriptan Benzoate ODT	Rizatriptan benzoate 10 mg/1	Tablet, Orally disintegratingOral	Direct Rx	72189-341	72189-0341-09

Other NDCs under ANDA 203146

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

FDA NDC Directory listings under ANDA 203146
Product	Strength	Form · route	Labeler	Product NDC
rizatriptan benzoate	Rizatriptan benzoate 5 mg/1	Tablet, Orally disintegratingOral	Macleods Pharmaceuticals Limited	33342-093
rizatriptan benzoate	Rizatriptan benzoate 10 mg/1	Tablet, Orally disintegratingOral	Macleods Pharmaceuticals Limited	33342-094