Package 67046-1597-3

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 67046-1597-3
Digits Only 6704615973
Product NDC 67046-1597
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1597-3)

Marketing

Marketing Status
Marketed Since 2025-09-18
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": "3f15c6c5-e94e-3ebd-e063-6394a90af7d1", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["3f15c889-4386-850b-e063-6294a90a8dbf"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1597-3)", "package_ndc": "67046-1597-3", "marketing_start_date": "20250918"}], "brand_name": "OXCARBAZEPINE", "product_id": "67046-1597_3f15c6c5-e94e-3ebd-e063-6394a90af7d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67046-1597", "generic_name": "OXCARBAZEPINE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20250918", "listing_expiration_date": "20261231"}