Package 69367-352-10
Brand: lacosamide
Generic: lacosamidePackage Facts
Identity
Package NDC
69367-352-10
Digits Only
6936735210
Product NDC
69367-352
Description
10 VIAL, GLASS in 1 CARTON (69367-352-10) / 20 mL in 1 VIAL, GLASS (69367-352-20)
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": ["INTRAVENOUS"], "spl_id": "89a391c2-4a46-47bc-976a-989442b47c56", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809974"], "spl_set_id": ["61e3747a-3957-4840-81f0-313aefbd5d2b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, GLASS in 1 CARTON (69367-352-10) / 20 mL in 1 VIAL, GLASS (69367-352-20)", "package_ndc": "69367-352-10", "marketing_start_date": "20250523"}], "brand_name": "Lacosamide", "product_id": "69367-352_89a391c2-4a46-47bc-976a-989442b47c56", "dosage_form": "INJECTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "69367-352", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA218706", "marketing_category": "ANDA", "marketing_start_date": "20250523", "listing_expiration_date": "20261231"}