Package 82983-427-31

Brand: lacosamide oral solution

Generic: lacosamide
NDC Package

Package Facts

Identity

Package NDC 82983-427-31
Digits Only 8298342731
Product NDC 82983-427
Description

200 mL in 1 BOTTLE, PLASTIC (82983-427-31)

Marketing

Marketing Status
Marketed Since 2025-07-14
Brand lacosamide oral solution
Generic lacosamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9fd5f392-f470-4f19-96da-582fae4da496", "openfda": {"nui": ["N0000008486"], "upc": ["0382983427310"], "unii": ["563KS2PQY5"], "rxcui": ["993856"], "spl_set_id": ["cb29da34-89aa-405a-8fbc-2308bda37187"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Ajenat Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE, PLASTIC (82983-427-31)", "package_ndc": "82983-427-31", "marketing_start_date": "20250714"}], "brand_name": "Lacosamide Oral Solution", "product_id": "82983-427_9fd5f392-f470-4f19-96da-582fae4da496", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "82983-427", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "Ajenat Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide Oral Solution", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA219699", "marketing_category": "ANDA", "marketing_start_date": "20250714", "listing_expiration_date": "20261231"}