Package 72162-1594-5

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 72162-1594-5
Digits Only 7216215945
Product NDC 72162-1594
Product ID 72162-1594_1cb3c3d3-ad1e-4c26-aa79-c38d98e21823
Description

500 TABLET, FILM COATED in 1 BOTTLE (72162-1594-5)

Marketing

Marketing Status
Marketed Since 2024-02-07
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": "1cb3c3d3-ad1e-4c26-aa79-c38d98e21823", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["d8edaa2b-3bab-4030-a4e3-0c77f7655731"], "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": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1594-1)", "package_ndc": "72162-1594-1", "marketing_start_date": "20240716"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1594-5)", "package_ndc": "72162-1594-5", "marketing_start_date": "20240207"}], "brand_name": "OXCARBAZEPINE", "product_id": "72162-1594_1cb3c3d3-ad1e-4c26-aa79-c38d98e21823", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-1594", "generic_name": "OXCARBAZEPINE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20080111", "listing_expiration_date": "20261231"}