Package 70518-3921-0

Brand: oxcarbazepine

Generic: oxcarbazepine
NDC Package

Package Facts

Identity

Package NDC 70518-3921-0
Digits Only 7051839210
Product NDC 70518-3921
Product ID 70518-3921_3646eab6-6f97-cf2b-e063-6294a90a1b93
Description

100 POUCH in 1 BOX (70518-3921-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-3921-1)

Marketing

Marketing Status
Marketed Since 2023-11-22
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": "3646eab6-6f97-cf2b-e063-6294a90a1b93", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["0abe9478-4084-286d-e063-6294a90a9ba7"], "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 (70518-3921-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-3921-1)", "package_ndc": "70518-3921-0", "marketing_start_date": "20231122"}], "brand_name": "Oxcarbazepine", "product_id": "70518-3921_3646eab6-6f97-cf2b-e063-6294a90a1b93", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-3921", "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": "ANDA215939", "marketing_category": "ANDA", "marketing_start_date": "20231122", "listing_expiration_date": "20261231"}