Package 63629-9186-1

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 63629-9186-1
Digits Only 6362991861
Product NDC 63629-9186
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-9186-1)

Marketing

Marketing Status
Marketed Since 2022-08-03
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": "1d4be567-97b8-4923-a2dd-8317e2d999d1", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["255f64ba-7667-48e6-8599-3b598bf6f4e9"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (63629-9186-1)", "package_ndc": "63629-9186-1", "marketing_start_date": "20220803"}], "brand_name": "OXCARBAZEPINE", "product_id": "63629-9186_1d4be567-97b8-4923-a2dd-8317e2d999d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-9186", "generic_name": "OXCARBAZEPINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20080111", "listing_expiration_date": "20261231"}