What is NDC 71335-2980?

71335-2980 is the product NDC for Rizatriptan, Rizatriptan benzoate 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 71335. 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?

4 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Rizatriptan NDC 71335-2980 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-2980Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-2980Add 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
71335-2980-1	7133529800171335298001	12 TABLET, FILM COATED in 1 BOTTLE (71335-2980-1)Marketed from Nov 26, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary): rizatriptan
Active ingredients: Rizatriptan benzoate — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 203147
Marketing start: Mar 11, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin 1b Receptor Agonists (Mechanism)Serotonin 1d Receptor Agonists (Mechanism)
Identifiers: Product ID 71335-2980_32eb56b6-9cb6-4ad2-bffb-1cf9af4bfd2dSPL ID 32eb56b6-9cb6-4ad2-bffb-1cf9af4bfd2dSPL set ID f000d96c-42a0-4aac-96ca-8cef289979ceRxCUI 314209UNII 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

N471335298001 followed by a unit qualifier and the quantity

Package 71335-2980-01. 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 Nov 26, 2025.

Indications (excerpt from the label)

Ri zatriptan benzoate 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 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 tablets, the diagnosis of migraine should be reconsidered before rizatriptan benzoate tablets are administered to treat any subsequent attacks. • Rizatriptan benzoate tablets are not indicated for use in the management of hemiplegic or basilar migraine [see Contraindications (4) ]. • Rizatriptan benzoate tablets are not i…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-2980

What is NDC 71335-2980?: 71335-2980 is the product NDC for Rizatriptan, Rizatriptan benzoate 10 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Rizatriptan.
What is the active ingredient?: Rizatriptan benzoate.
Who is the labeler?: Bryant Ranch Prepack, NDC labeler code 71335. 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?: 4 other product NDCs are listed under this name. See all Rizatriptan 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Rizatriptan	Rizatriptan benzoate 5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-087	33342-0087-0733342-0087-1233342-0087-41+4 more
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-088	33342-0088-0733342-0088-1233342-0088-41+4 more
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7747	50090-7747-00
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1352	71335-1352-0171335-1352-0271335-1352-03+4 more

Other NDCs under ANDA 203147

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

FDA NDC Directory listings under ANDA 203147
Product	Strength	Form · route	Labeler	Product NDC
Rizatriptan	Rizatriptan benzoate 5 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-087
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	Macleods Pharmaceuticals Limited	33342-088
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7747
Rizatriptan	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1352
Rizatriptan Benzoate	Rizatriptan benzoate 10 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-447