Package 70518-2370-2

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 70518-2370-2
Digits Only 7051823702
Product NDC 70518-2370
Product ID 70518-2370_4a063c48-af90-6642-e063-6394a90addc4
Description

100 POUCH in 1 BOX (70518-2370-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-3)

Marketing

Marketing Status
Marketed Since 2024-10-04
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": "4a063c48-af90-6642-e063-6394a90addc4", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["ffc8d10c-0049-4fe5-beb8-79cc6a197ede"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2370-2)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2370-3)", "package_ndc": "70518-2370-2", "marketing_start_date": "20241004"}], "brand_name": "OXCARBAZEPINE", "product_id": "70518-2370_4a063c48-af90-6642-e063-6394a90addc4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2370", "generic_name": "OXCARBAZEPINE", "labeler_name": "REMEDYREPACK INC.", "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": "20191019", "listing_expiration_date": "20271231"}