Package 10135-799-86
Brand: lacosamide
Generic: lacosamidePackage Facts
Identity
Package NDC
10135-799-86
Digits Only
1013579986
Product NDC
10135-799
Description
6 BLISTER PACK in 1 CARTON (10135-799-86) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
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": "67afbd17-4406-4e18-a302-c0a5829ec903", "openfda": {"nui": ["N0000008486"], "upc": ["0310135800605", "0310135799602", "0310135802609"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["0a273024-c2d2-4fae-90c3-b2f38a323f24"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-799-60)", "package_ndc": "10135-799-60", "marketing_start_date": "20250701"}, {"sample": false, "description": "6 BLISTER PACK in 1 CARTON (10135-799-86) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "10135-799-86", "marketing_start_date": "20250701"}], "brand_name": "Lacosamide", "product_id": "10135-799_67afbd17-4406-4e18-a302-c0a5829ec903", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "10135-799", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Marlex Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "50 mg/1"}], "application_number": "ANDA218014", "marketing_category": "ANDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}