What is NDC 62756-520?

62756-520 is the product NDC for sumatriptan succinate, Sumatriptan succinate 25 mg/1 tablet, film coated, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. 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 62756-520 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62756-520Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62756-0520Add 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
62756-520-01	62756052001	3 BLISTER PACK in 1 CARTON (62756-520-01) / 9 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Nov 1, 2020
62756-520-08	62756052008	100 TABLET, FILM COATED in 1 BOTTLE (62756-520-08)Marketed from Aug 10, 2009
62756-520-18	62756052018	1000 TABLET, FILM COATED in 1 BOTTLE (62756-520-18)Marketed from Aug 10, 2009
62756-520-83	62756052083	30 TABLET, FILM COATED in 1 BOTTLE (62756-520-83)Marketed from Aug 10, 2009
62756-520-93	62756052093	9 BLISTER PACK in 1 CARTON (62756-520-93) / 1 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Aug 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 succinate
Generic name (nonproprietary): sumatriptan succinate
Active ingredients: Sumatriptan succinate — 25 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Sun Pharmaceutical Industries, Inc.NDC labeler code 62756
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078295
Marketing start: Aug 10, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 62756-520_55125fc1-837d-05ea-e063-6394a90a57caSPL ID 55125fc1-837d-05ea-e063-6394a90a57caSPL set ID 9485cc30-15e8-4b53-876d-db317145474bUNII J8BDZ68989UPC 0362756521889, 0362756522886
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

N462756052001 followed by a unit qualifier and the quantity

Package 62756-0520-01. 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 Jun 25, 2026.

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. Sumatriptan succinate is a serotonin (5-HT 1B/1D ) receptor agonist (tripta…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62756-520

What is NDC 62756-520?: 62756-520 is the product NDC for sumatriptan succinate, Sumatriptan succinate 25 mg/1 tablet, film coated, listed with the FDA by Sun Pharmaceutical Industries, Inc.. It has 5 package NDCs, 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?: Sun Pharmaceutical Industries, Inc., NDC labeler code 62756. 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 6 mg/.5mL	InjectionSubcutaneous	Alembic Pharmaceuticals Limited	46708-657	46708-0657-0146708-0657-05
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	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	Sportpharm LLC	85766-238	85766-0238-02
Sumatriptan Succinate	Sumatriptan succinate 6 mg/.5mL	InjectionSubcutaneous	Dr. Reddys Laboratories Inc.,	43598-768	43598-0768-23
Sumatriptan Succinate	Sumatriptan succinate 25 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-432	72189-0432-09

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 25 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-432
Sumatriptan Succinate	Sumatriptan succinate 50 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-433
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