Package 31722-024-01
Brand: oxcarbazepine
Generic: oxcarbazepinePackage Facts
Identity
Package NDC
31722-024-01
Digits Only
3172202401
Product NDC
31722-024
Description
100 TABLET, FILM COATED in 1 BOTTLE (31722-024-01)
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": "4998217b-01c6-d647-e063-6294a90a2ff9", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0331722023054", "0331722024051", "0331722025058"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["fe49a773-562c-4da6-96b7-bba52f4d61e2"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-024-01)", "package_ndc": "31722-024-01", "marketing_start_date": "20220111"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-024-05)", "package_ndc": "31722-024-05", "marketing_start_date": "20230310"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (31722-024-10)", "package_ndc": "31722-024-10", "marketing_start_date": "20230310"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-024-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "31722-024-31", "marketing_start_date": "20220111"}], "brand_name": "Oxcarbazepine", "product_id": "31722-024_4998217b-01c6-d647-e063-6294a90a2ff9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-024", "generic_name": "Oxcarbazepine", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA215939", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20271231"}