lacosamide

Generic: lacosamide

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

Drug Facts

Product Profile

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

lacosamide 100 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-172
Product ID 62332-172_50c42e50-ab11-460a-a8f6-0edcd1b91613
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204974
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2022-03-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332172
Hyphenated Format 62332-172

Supplemental Identifiers

RxCUI
809987 809992 809996 810000
UPC
0362332172306
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 ANDA204974 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (62332-172-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (62332-172-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (62332-172-60)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62332-172-91)
source: ndc

Packages (4)

62332-172-10 100 BLISTER PACK in 1 CARTON (62332-172-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK 62332-172-30 30 TABLET, FILM COATED in 1 BOTTLE (62332-172-30) 62332-172-60 60 TABLET, FILM COATED in 1 BOTTLE (62332-172-60) 62332-172-91 1000 TABLET, FILM COATED in 1 BOTTLE (62332-172-91)

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": "50c42e50-ab11-460a-a8f6-0edcd1b91613", "openfda": {"nui": ["N0000008486"], "upc": ["0362332172306"], "unii": ["563KS2PQY5"], "rxcui": ["809987", "809992", "809996", "810000"], "spl_set_id": ["07b7b3f2-16a0-4deb-883b-10522676d966"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (62332-172-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62332-172-10", "marketing_start_date": "20220318"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62332-172-30)", "package_ndc": "62332-172-30", "marketing_start_date": "20220318"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62332-172-60)", "package_ndc": "62332-172-60", "marketing_start_date": "20220318"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62332-172-91)", "package_ndc": "62332-172-91", "marketing_start_date": "20220318"}], "brand_name": "Lacosamide", "product_id": "62332-172_50c42e50-ab11-460a-a8f6-0edcd1b91613", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "62332-172", "dea_schedule": "CV", "generic_name": "lacosamide", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "100 mg/1"}], "application_number": "ANDA204974", "marketing_category": "ANDA", "marketing_start_date": "20220318", "listing_expiration_date": "20261231"}