Package 72603-305-01

Brand: lacosamide

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 72603-305-01
Digits Only 7260330501
Product NDC 72603-305
Product ID 72603-305_e70388c9-39ef-4803-8a10-d46902a45462
Description

200 mL in 1 BOTTLE, PLASTIC (72603-305-01)

Marketing

Marketing Status
Marketed Since 2024-06-01
Brand lacosamide
Generic lacosamide
Sample Package No

Linked Drug Pages (1)

Lacosamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e70388c9-39ef-4803-8a10-d46902a45462", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["993856"], "spl_set_id": ["48fcaa27-baaa-446e-a282-0c3e232cd151"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE, PLASTIC (72603-305-01)", "package_ndc": "72603-305-01", "marketing_start_date": "20240601"}], "brand_name": "Lacosamide", "product_id": "72603-305_e70388c9-39ef-4803-8a10-d46902a45462", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72603-305", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA209224", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}