Package 62756-259-03

Brand: zonisamide

Generic: zonisamide
NDC Package

Package Facts

Identity

Package NDC 62756-259-03
Digits Only 6275625903
Product NDC 62756-259
Description

100 CAPSULE in 1 BOTTLE (62756-259-03)

Marketing

Marketing Status
Marketed Since 2006-03-17
Brand zonisamide
Generic zonisamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d0c9002b-fa32-4ca8-862f-5286746df2cb", "openfda": {"nui": ["N0000175753", "N0000008486", "M0020790", "N0000000235", "N0000185503"], "upc": ["0362756260016", "0362756259010", "0362756258013"], "unii": ["459384H98V"], "rxcui": ["314285", "403966", "403967"], "spl_set_id": ["3164d438-90bf-420a-9a56-5498b987f91c"], "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": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (62756-259-01)", "package_ndc": "62756-259-01", "marketing_start_date": "20060317"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-259-02)", "package_ndc": "62756-259-02", "marketing_start_date": "20060317"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (62756-259-03)", "package_ndc": "62756-259-03", "marketing_start_date": "20060317"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (62756-259-04)", "package_ndc": "62756-259-04", "marketing_start_date": "20060317"}], "brand_name": "Zonisamide", "product_id": "62756-259_d0c9002b-fa32-4ca8-862f-5286746df2cb", "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": "62756-259", "generic_name": "Zonisamide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zonisamide", "active_ingredients": [{"name": "ZONISAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA077634", "marketing_category": "ANDA", "marketing_start_date": "20060317", "listing_expiration_date": "20261231"}