Package 72888-089-05

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 72888-089-05
Digits Only 7288808905
Product NDC 72888-089
Description

500 TABLET, FILM COATED in 1 BOTTLE (72888-089-05)

Marketing

Marketing Status
Marketed Since 2021-03-19
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": "4b920b8e-b260-b6a0-e063-6294a90a3490", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0372888088303", "0372888088013", "0372888089058", "0372888089300", "0372888087016", "0372888087054", "0372888088051", "0372888087306", "0372888089010"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["b0bc10f0-7d1b-4adc-bc59-c48dab58ee5a"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72888-089-01)", "package_ndc": "72888-089-01", "marketing_start_date": "20210319"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72888-089-05)", "package_ndc": "72888-089-05", "marketing_start_date": "20210319"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72888-089-30)", "package_ndc": "72888-089-30", "marketing_start_date": "20210319"}], "brand_name": "Oxcarbazepine", "product_id": "72888-089_4b920b8e-b260-b6a0-e063-6294a90a3490", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72888-089", "generic_name": "oxcarbazepine", "labeler_name": "Advagen Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "600 mg/1"}], "application_number": "ANDA077747", "marketing_category": "ANDA", "marketing_start_date": "20210319", "listing_expiration_date": "20271231"}