Package 85742-010-08

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 85742-010-08
Digits Only 8574201008
Product NDC 85742-010
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85742-010-08)

Marketing

Marketing Status
Marketed Since 2025-10-06
Brand lacosamide
Generic lacosamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9e55b694-312b-480c-a20f-a6ed325906d7", "openfda": {"nui": ["N0000008486"], "upc": ["0385742009086", "0385742008089", "0385742010082", "0385742008072", "0385742011089"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["5c03b90e-6985-4005-b6c5-44626d0600d7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Kanchan Healthcare Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 BLISTER PACK in 1 CARTON (85742-010-07)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "85742-010-07", "marketing_start_date": "20251006"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85742-010-08)", "package_ndc": "85742-010-08", "marketing_start_date": "20251006"}], "brand_name": "Lacosamide", "product_id": "85742-010_9e55b694-312b-480c-a20f-a6ed325906d7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "85742-010", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Kanchan Healthcare Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "150 mg/1"}], "application_number": "ANDA218014", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}