Package 63629-3816-3

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 63629-3816-3
Digits Only 6362938163
Product NDC 63629-3816
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-3816-3)

Marketing

Marketing Status
Marketed Since 2012-08-06
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": "e1e371c0-49d4-401e-8e7c-b953f579480e", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["78f196d4-110e-45b1-813a-725f52c1a4eb"], "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": "30 TABLET, FILM COATED in 1 BOTTLE (63629-3816-1)", "package_ndc": "63629-3816-1", "marketing_start_date": "20110728"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-3816-2)", "package_ndc": "63629-3816-2", "marketing_start_date": "20081014"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-3816-3)", "package_ndc": "63629-3816-3", "marketing_start_date": "20120806"}], "brand_name": "OXCARBAZEPINE", "product_id": "63629-3816_e1e371c0-49d4-401e-8e7c-b953f579480e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-3816", "generic_name": "OXCARBAZEPINE", "labeler_name": "Bryant Ranch Prepack", "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": "20080111", "listing_expiration_date": "20261231"}