lacosamide

Generic: lacosamide

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lacosamide
Generic Name lacosamide
Labeler american health packaging
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lacosamide 10 mg/mL

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-847
Product ID 60687-847_3140053a-3d5f-f403-e063-6394a90a6d37
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209224
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2025-01-09

Pharmacologic Class

Physiologic Effect
decreased central nervous system disorganized electrical activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687847
Hyphenated Format 60687-847

Supplemental Identifiers

RxCUI
993856
UNII
563KS2PQY5
NUI
N0000008486

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lacosamide (source: ndc)
Generic Name lacosamide (source: ndc)
Application Number ANDA209224 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 TRAY in 1 CASE (60687-847-54) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-847-40)
  • 1 TRAY in 1 CASE (60687-847-55) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-48) / 10 mL in 1 CUP, UNIT-DOSE (60687-847-42)
  • 1 TRAY in 1 CASE (60687-847-82) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-53) / 20 mL in 1 CUP, UNIT-DOSE (60687-847-24)
source: ndc

Packages (3)

Ingredients (1)

lacosamide (10 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3140053a-3d5f-f403-e063-6394a90a6d37", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["993856"], "spl_set_id": ["f9aa6154-5d80-4597-90c3-cec131b455d4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "1 TRAY in 1 CASE (60687-847-54)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-46)  / 5 mL in 1 CUP, UNIT-DOSE (60687-847-40)", "package_ndc": "60687-847-54", "marketing_start_date": "20250124"}, {"sample": false, "description": "1 TRAY in 1 CASE (60687-847-55)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-48)  / 10 mL in 1 CUP, UNIT-DOSE (60687-847-42)", "package_ndc": "60687-847-55", "marketing_start_date": "20250113"}, {"sample": false, "description": "1 TRAY in 1 CASE (60687-847-82)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-847-53)  / 20 mL in 1 CUP, UNIT-DOSE (60687-847-24)", "package_ndc": "60687-847-82", "marketing_start_date": "20250109"}], "brand_name": "Lacosamide", "product_id": "60687-847_3140053a-3d5f-f403-e063-6394a90a6d37", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60687-847", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "American Health Packaging", "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": "20250109", "listing_expiration_date": "20261231"}