Package 63629-6834-2
Brand: oxcarbazepine
Generic: oxcarbazepinePackage Facts
Identity
Package NDC
63629-6834-2
Digits Only
6362968342
Product NDC
63629-6834
Description
60 TABLET, FILM COATED in 1 BOTTLE (63629-6834-2)
Marketing
Marketing Status
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": "ad785cbb-ae12-4261-9fb2-a86b8735606d", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312138"], "spl_set_id": ["d3c7a3b8-b9a2-4a5f-98b3-0ed02eca3433"], "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 (63629-6834-1)", "package_ndc": "63629-6834-1", "marketing_start_date": "20160627"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63629-6834-2)", "package_ndc": "63629-6834-2", "marketing_start_date": "20151102"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-6834-3)", "package_ndc": "63629-6834-3", "marketing_start_date": "20160713"}], "brand_name": "OXCARBAZEPINE", "product_id": "63629-6834_ad785cbb-ae12-4261-9fb2-a86b8735606d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-6834", "generic_name": "OXCARBAZEPINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "600 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20080111", "listing_expiration_date": "20261231"}