What is NDC 71335-0962?

71335-0962 is the product NDC for Zonisamide, Zonisamide 50 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, 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 Zonisamide?

47 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Zonisamide NDC 71335-0962 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-0962Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-0962Add 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
71335-0962-1	71335096201	30 CAPSULE in 1 BOTTLE (71335-0962-1)Marketed from Sep 11, 2020
71335-0962-2	71335096202	60 CAPSULE in 1 BOTTLE (71335-0962-2)Marketed from Oct 5, 2018
71335-0962-3	71335096203	90 CAPSULE in 1 BOTTLE (71335-0962-3)Marketed from Jan 28, 2022
71335-0962-4	71335096204	120 CAPSULE in 1 BOTTLE (71335-0962-4)Marketed from Jan 28, 2022

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): Zonisamide
Generic name (nonproprietary): zonisamide
Active ingredients: Zonisamide — 50 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 71335
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077634
Marketing start: Mar 17, 2006
Listing expires: Dec 31, 2027
Other FDA classes: Carbonic Anhydrase Inhibitors (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)P-Glycoprotein Inhibitors (Mechanism)Sulfonamides (Chemical structure)
Identifiers: Product ID 71335-0962_c4d106a8-f261-456c-838e-483dcb4483d3SPL ID c4d106a8-f261-456c-838e-483dcb4483d3SPL set ID 467a73f0-1cd1-46bf-83b3-ee38badb761cRxCUI 403967UNII 459384H98V
Pharmacologic class: Anti-epileptic Agent

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

N471335096201 followed by a unit qualifier and the quantity

Package 71335-0962-01. 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 Jul 14, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Zonisamide is indicated as adjunctive therapy in the treatment of partial seizures in adults with epilepsy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-0962

What is NDC 71335-0962?: 71335-0962 is the product NDC for Zonisamide, Zonisamide 50 mg/1 capsule, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Zonisamide.
What is the active ingredient?: Zonisamide.
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 Zonisamide?: 47 other product NDCs are listed under this name. See all Zonisamide 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 Zonisamide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4600	70518-4600-0070518-4600-02
Zonisamide	Zonisamide 50 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-4349	70518-4349-00
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	Direct_Rx	72189-624	72189-0624-72
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Advanced Rx Pharmacy of Tennessee, LLC	80425-0392	80425-0392-0180425-0392-02
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Advanced Rx of Tennessee, LLC	80425-0370	80425-0370-01
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	REMEDYREPACK INC.	70518-3903	70518-3903-00
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	Direct_Rx	72189-374	72189-0374-72
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	Viona Pharmaceuticals Inc	72578-040	72578-0040-0172578-0040-05
Zonisamide	Zonisamide 50 mg/1	CapsuleOral	Viona Pharmaceuticals Inc	72578-041	72578-0041-0172578-0041-05
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Viona Pharmaceuticals Inc	72578-042	72578-0042-0172578-0042-0572578-0042-10

All 48 Zonisamide NDCs

Other NDCs under ANDA 077634

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

FDA NDC Directory listings under ANDA 077634
Product	Strength	Form · route	Labeler	Product NDC
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Proficient Rx LP	63187-897
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	Direct_Rx	72189-374
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Bryant Ranch Prepack	63629-3293
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Preferred Pharmaceuticals, Inc.	68788-7438
Zonisamide	Zonisamide 50 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-259
Zonisamide	Zonisamide 25 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-258
Zonisamide	Zonisamide 100 mg/1	CapsuleOral	Sun Pharmaceutical Industries, Inc.	62756-260