Package 72189-339-60

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 72189-339-60
Digits Only 7218933960
Product NDC 72189-339
Product ID 72189-339_2c4c3e43-2d44-28b3-e063-6394a90a306a
Description

60 TABLET, FILM COATED in 1 BOTTLE (72189-339-60)

Marketing

Marketing Status
Marketed Since 2022-04-05
Brand oxcarbazepine
Generic oxcarbazepine
Sample Package No

Linked Drug Pages (1)

OXCARBAZEPINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4c3e43-2d44-28b3-e063-6394a90a306a", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["dbea45c2-e166-b557-e053-2995a90a7643"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-339-60)", "package_ndc": "72189-339-60", "marketing_start_date": "20220405"}], "brand_name": "OXCARBAZEPINE", "product_id": "72189-339_2c4c3e43-2d44-28b3-e063-6394a90a306a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-339", "generic_name": "OXCARBAZEPINE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA077794", "marketing_category": "ANDA", "marketing_start_date": "20220405", "listing_expiration_date": "20261231"}