What is NDC 63304-099?

63304-099 is the product NDC for Sumatriptan, Sumatriptan succinate 100 mg/1 tablet, listed with the FDA by SUN PHARMACEUTICAL INDUSTRIES, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

SUN PHARMACEUTICAL INDUSTRIES, INC., NDC labeler code 63304. 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?

72 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sumatriptan NDC 63304-099 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63304-099Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63304-0099Add 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
63304-099-13	63304009913	120 TABLET in 1 BOTTLE (63304-099-13)Marketed from Feb 10, 2009
63304-099-19	63304009919	1 BLISTER PACK in 1 CARTON (63304-099-19) / 9 TABLET in 1 BLISTER PACKMarketed from Feb 10, 2009
63304-099-45	63304009945	5 TABLET in 1 BOTTLE (63304-099-45)Marketed from Feb 10, 2009

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
Generic name (nonproprietary): sumatriptan
Active ingredients: Sumatriptan succinate — 100 mg/1
Dosage form: Tablet
Route: Oral
Labeler: SUN PHARMACEUTICAL INDUSTRIES, INC.NDC labeler code 63304
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076572
Marketing start: Feb 10, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 63304-099_9bc4f2da-41f0-42e2-98b2-b689c02d0a3eSPL ID 9bc4f2da-41f0-42e2-98b2-b689c02d0a3eSPL set ID c87cf537-9f7f-400e-ac4b-86e6f7e78775RxCUI 313160, 313161, 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

N463304009913 followed by a unit qualifier and the quantity

Package 63304-0099-13. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 63304-099

What is NDC 63304-099?: 63304-099 is the product NDC for Sumatriptan, Sumatriptan succinate 100 mg/1 tablet, listed with the FDA by SUN PHARMACEUTICAL INDUSTRIES, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sumatriptan.
What is the active ingredient?: Sumatriptan succinate.
Who is the labeler?: SUN PHARMACEUTICAL INDUSTRIES, INC., NDC labeler code 63304. 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?: 72 other product NDCs are listed under this name. See all Sumatriptan 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	Armas Pharmaceuticals Inc.	72485-518	72485-0518-05
Sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	Strides Pharma Science Limited	64380-740	64380-0740-0164380-0740-02
sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	ONESOURCE SPECIALTY PHARMA LIMITED	83270-151	83270-0151-07
sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	ONESOURCE SPECIALTY PHARMA LIMITED	83270-152	83270-0152-07
sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	ONESOURCE SPECIALTY PHARMA LIMITED	83270-005	83270-0005-01
sumatriptan	Sumatriptan succinate 25 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	64980-660	64980-0660-2764980-0660-3664980-0660-91
sumatriptan	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	64980-661	64980-0661-2764980-0661-3664980-0661-91
sumatriptan	Sumatriptan succinate 100 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	64980-662	64980-0662-2764980-0662-3664980-0662-91
Sumatriptan	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Advanced Rx of Tennessee, LLC	80425-0475	80425-0475-01
Sumatriptan	Sumatriptan succinate 6 mg/.5mL	Injection, SolutionSubcutaneous	A-S Medication Solutions	50090-7957	50090-7957-00

All 73 Sumatriptan NDCs

Other NDCs under ANDA 076572

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

FDA NDC Directory listings under ANDA 076572
Product	Strength	Form · route	Labeler	Product NDC
Sumatriptan	Sumatriptan succinate 100 mg/1	TabletOral	Proficient Rx LP	63187-323