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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lacosamide 50 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 60687-676
Product ID 60687-676_4c5d9cc4-2e98-ae84-e063-6394a90af1d6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214695
DEA Schedule cv
Listing Expiration 2027-12-31
Marketing Start 2022-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60687676
Hyphenated Format 60687-676

Supplemental Identifiers

RxCUI
809987 809996 810000
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 ANDA214695 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 BLISTER PACK in 1 CARTON (60687-676-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)
source: ndc

Packages (1)

60687-676-57 60 BLISTER PACK in 1 CARTON (60687-676-57) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)

Ingredients (1)

lacosamide (50 mg/1)

Linked Drug Pages (1)

Lacosamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4c5d9cc4-2e98-ae84-e063-6394a90af1d6", "openfda": {"nui": ["N0000008486"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809996", "810000"], "spl_set_id": ["19060029-c158-4a37-9261-cfe3b2b5b1e3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "60 BLISTER PACK in 1 CARTON (60687-676-57)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-676-11)", "package_ndc": "60687-676-57", "marketing_start_date": "20220601"}], "brand_name": "Lacosamide", "product_id": "60687-676_4c5d9cc4-2e98-ae84-e063-6394a90af1d6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "60687-676", "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": "50 mg/1"}], "application_number": "ANDA214695", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20271231"}