What is NDC 71921-170?

71921-170 is the product NDC for Sumatriptan, Sumatriptan 20 mg/1 spray, listed with the FDA by Florida Pharmaceutical Products, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.

Florida Pharmaceutical Products, LLC., NDC labeler code 71921. 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?

75 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 71921-170 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71921-170Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71921-0170Add 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
71921-170-61	7192101706171921017061	6 CONTAINER in 1 BOX (71921-170-61) / 1 SPRAY in 1 CONTAINERMarketed from May 15, 2021

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 — 20 mg/1
Dosage form: Spray
Route: Nasal
Labeler: Florida Pharmaceutical Products, LLC.NDC labeler code 71921
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208967
Marketing start: May 15, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 71921-170_d0b56323-49ef-f239-e053-2a95a90ae766SPL ID d0b56323-49ef-f239-e053-2a95a90ae766SPL set ID 267dadc1-6960-4d8b-88ef-86be9c5f7159RxCUI 314227UNII 8R78F6L9VO
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. Nasal products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471921017061 followed by a unit qualifier and the quantity

Package 71921-0170-61. 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 Nov 13, 2021.

Indications (excerpt from the label)

Sumatriptan nasal spray is 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 nasal spray, reconsider the diagnosis of migraine before Sumatriptan nasal spray is administered to treat any subsequent attacks. Sumatriptan is not indicated for the prevention of migraine attacks. Safety and effectiveness of sumatriptan nasal spray have not been established for cluster headache. Sumatriptan is a serotonin (5-HT 1B/1D ) receptor agonist (triptan) indicated for acute treatment of migraine with or wi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71921-170

What is NDC 71921-170?: 71921-170 is the product NDC for Sumatriptan, Sumatriptan 20 mg/1 spray, listed with the FDA by Florida Pharmaceutical Products, LLC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sumatriptan.
What is the active ingredient?: Sumatriptan.
Who is the labeler?: Florida Pharmaceutical Products, LLC., NDC labeler code 71921. 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?: 75 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	A-S Medication Solutions	50090-8109	50090-8109-00
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

All 76 Sumatriptan NDCs