lacosamide

Generic: lacosamide

Labeler: camber pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lacosamide
Generic Name lacosamide
Labeler camber pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

lacosamide 100 mg/1

Manufacturer
Camber Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 31722-813
Product ID 31722-813_38389544-6f70-6dd3-e063-6394a90ad1e0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204787
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2022-03-17

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 31722813
Hyphenated Format 31722-813

Supplemental Identifiers

RxCUI
809987 809992 809996 810000
UPC
0331722815604 0331722813600 0331722814607 0331722812603
UNII
563KS2PQY5
NUI
N0000008486

Packaging Origin

Original Packager
true

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 ANDA204787 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE (31722-813-05)
  • 180 TABLET, FILM COATED in 1 BOTTLE (31722-813-18)
  • 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-813-32)
  • 60 TABLET, FILM COATED in 1 BOTTLE (31722-813-60)
source: ndc

Packages (4)

31722-813-05 500 TABLET, FILM COATED in 1 BOTTLE (31722-813-05) 31722-813-18 180 TABLET, FILM COATED in 1 BOTTLE (31722-813-18) 31722-813-32 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-813-32) 31722-813-60 60 TABLET, FILM COATED in 1 BOTTLE (31722-813-60)

Ingredients (1)

lacosamide (100 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": "38389544-6f70-6dd3-e063-6394a90ad1e0", "openfda": {"nui": ["N0000008486"], "upc": ["0331722815604", "0331722813600", "0331722814607", "0331722812603"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["c5b91128-f838-4e98-9684-5f477fc7af06"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-813-05)", "package_ndc": "31722-813-05", "marketing_start_date": "20220317"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (31722-813-18)", "package_ndc": "31722-813-18", "marketing_start_date": "20220317"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BLISTER PACK (31722-813-32)", "package_ndc": "31722-813-32", "marketing_start_date": "20220317"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-813-60)", "package_ndc": "31722-813-60", "marketing_start_date": "20220317"}], "brand_name": "LACOSAMIDE", "product_id": "31722-813_38389544-6f70-6dd3-e063-6394a90ad1e0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-813", "dea_schedule": "CV", "generic_name": "LACOSAMIDE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LACOSAMIDE", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA204787", "marketing_category": "ANDA", "marketing_start_date": "20220317", "listing_expiration_date": "20261231"}