What is NDC 72189-432?

72189-432 is the product NDC for Sumatriptan Succinate, Sumatriptan succinate 25 mg/1 tablet, film coated, 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 Sumatriptan Succinate?

34 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sumatriptan Succinate NDC 72189-432 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-432Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0432Add 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
72189-432-09	72189043209	9 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)Marketed from Mar 13, 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): Sumatriptan Succinate
Generic name (nonproprietary): sumatriptan succinate
Active ingredients: Sumatriptan succinate — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078295
Marketing start: Mar 13, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 72189-432_2c4d7702-337b-5298-e063-6394a90a7f3bSPL ID 2c4d7702-337b-5298-e063-6394a90a7f3bSPL set ID f6c95873-576d-a1c2-e053-6294a90a3ff9RxCUI 315223UNII J8BDZ68989
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

N472189043209 followed by a unit qualifier and the quantity

Package 72189-0432-09. 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 22, 2025.

Indications (excerpt from the label)

Sumatriptan succinate tablets are indicated for the acute treatment of migraine with or without aura in adults. Limitations of Use: Use only if a clear diagnosis of migraine headache has been established. If a patient has no response to the first migraine attack treated with sumatriptan succinate tablets, reconsider the diagnosis of migraine before sumatriptan succinate tablets are administered to treat any subsequent attacks. Sumatriptan succinate tablets are not indicated for the prevention of migraine attacks. Safety and effectiveness of sumatriptan succinate tablets have not been established for cluster headache.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-432

What is NDC 72189-432?: 72189-432 is the product NDC for Sumatriptan Succinate, Sumatriptan succinate 25 mg/1 tablet, film coated, 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?: Sumatriptan Succinate.
What is the active ingredient?: Sumatriptan succinate.
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 Sumatriptan Succinate?: 34 other product NDCs are listed under this name. See all Sumatriptan Succinate 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 Sumatriptan Succinate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sumatriptan Succinate	Sumatriptan succinate 4 mg/.5mL	InjectionSubcutaneous	Alembic Pharmaceuticals Inc.	62332-656	62332-0656-0162332-0656-05
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Alembic Pharmaceuticals Inc.	62332-657	62332-0657-0162332-0657-05
Sumatriptan Succinate	Sumatriptan succinate 4 mg/.5mL	InjectionSubcutaneous	Alembic Pharmaceuticals Limited	46708-656	46708-0656-0146708-0656-05
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Alembic Pharmaceuticals Limited	46708-657	46708-0657-0146708-0657-05
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Sun Pharmaceutical Industries, Inc.	47335-276	47335-0276-4047335-0276-41
Sumatriptan Succinate	Sumatriptan succinate 25 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-596	72189-0596-09
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	NorthStar Rx LLC	72603-141	72603-0141-02
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Dr. Reddys Laboratories Inc.,	43598-768	43598-0768-23
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Sportpharm LLC	85766-238	85766-0238-02
Sumatriptan Succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-433	72189-0433-09

All 35 Sumatriptan Succinate NDCs

Other NDCs under ANDA 078295

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

FDA NDC Directory listings under ANDA 078295
Product	Strength	Form · route	Labeler	Product NDC
sumatriptan succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-251
sumatriptan succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-274
sumatriptan succinate	Sumatriptan succinate 25 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-5939
Sumatriptan Succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-433
sumatriptan succinate	Sumatriptan succinate 25 mg/1	Tablet, Film coatedOral	Sun Pharmaceutical Industries, Inc.	62756-520
sumatriptan succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Sun Pharmaceutical Industries, Inc.	62756-521
sumatriptan succinate	Sumatriptan succinate 100 mg/1	Tablet, Film coatedOral	Sun Pharmaceutical Industries, Inc.	62756-522