Package 68382-692-10

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 68382-692-10
Digits Only 6838269210
Product NDC 68382-692
Description

1000 TABLET in 1 BOTTLE (68382-692-10)

Marketing

Marketing Status
Marketed Since 2025-07-10
Brand oxcarbazepine
Generic oxcarbazepine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f743cc83-a47d-4a48-8be5-516be5c7d7e8", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0368382692306", "0368382691309", "0368382693013", "0368382693303", "0368382692016", "0368382691019"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["5048dc87-2d89-434d-be51-4a97b0ce0601"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-692-01)", "package_ndc": "68382-692-01", "marketing_start_date": "20250710"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-692-05)", "package_ndc": "68382-692-05", "marketing_start_date": "20250710"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-692-10)", "package_ndc": "68382-692-10", "marketing_start_date": "20250710"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68382-692-30)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "68382-692-30", "marketing_start_date": "20250710"}], "brand_name": "oxcarbazepine", "product_id": "68382-692_f743cc83-a47d-4a48-8be5-516be5c7d7e8", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68382-692", "generic_name": "oxcarbazepine", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA211747", "marketing_category": "ANDA", "marketing_start_date": "20250710", "listing_expiration_date": "20261231"}