zonisamide

Generic: zonisamide

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zonisamide
Generic Name zonisamide
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

zonisamide 25 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-374
Product ID 72189-374_2c4cbd73-cdad-14f5-e063-6294a90ab38e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077634
Listing Expiration 2026-12-31
Marketing Start 2022-08-15

Pharmacologic Class

Established (EPC)
anti-epileptic agent [epc]
Mechanism of Action
carbonic anhydrase inhibitors [moa] p-glycoprotein inhibitors [moa]
Chemical Structure
sulfonamides [cs]
Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189374
Hyphenated Format 72189-374

Supplemental Identifiers

RxCUI
403966
UNII
459384H98V
NUI
N0000175753 N0000008486 M0020790 N0000000235 N0000185503

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zonisamide (source: ndc)
Generic Name zonisamide (source: ndc)
Application Number ANDA077634 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 120 CAPSULE in 1 BOTTLE (72189-374-72)
source: ndc

Packages (1)

72189-374-72 120 CAPSULE in 1 BOTTLE (72189-374-72)

Ingredients (1)

zonisamide (25 mg/1)

Linked Drug Pages (1)

Zonisamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4cbd73-cdad-14f5-e063-6294a90ab38e", "openfda": {"nui": ["N0000175753", "N0000008486", "M0020790", "N0000000235", "N0000185503"], "unii": ["459384H98V"], "rxcui": ["403966"], "spl_set_id": ["e64b78d8-79de-337b-e053-2a95a90a4861"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]", "P-Glycoprotein Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE in 1 BOTTLE (72189-374-72)", "package_ndc": "72189-374-72", "marketing_start_date": "20220815"}], "brand_name": "Zonisamide", "product_id": "72189-374_2c4cbd73-cdad-14f5-e063-6294a90ab38e", "dosage_form": "CAPSULE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "P-Glycoprotein Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "72189-374", "generic_name": "Zonisamide", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zonisamide", "active_ingredients": [{"name": "ZONISAMIDE", "strength": "25 mg/1"}], "application_number": "ANDA077634", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}