lacosamide

Generic: lacosamide

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

Drug Facts

Product Profile

Brand Name lacosamide
Generic Name lacosamide
Labeler ani pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

lacosamide 10 mg/mL

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-488
Product ID 70954-488_8b5b4014-2795-4ebd-b53e-1157a2c0b98a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216151
DEA Schedule cv
Listing Expiration 2026-12-31
Marketing Start 2022-08-26

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70954488
Hyphenated Format 70954-488

Supplemental Identifiers

RxCUI
993856
UPC
0370954488101
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 ANDA216151 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 200 mL in 1 BOTTLE, PLASTIC (70954-488-10)
source: ndc

Packages (1)

70954-488-10 200 mL in 1 BOTTLE, PLASTIC (70954-488-10)

Ingredients (1)

lacosamide (10 mg/mL)

Linked Drug Pages (1)

Lacosamide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8b5b4014-2795-4ebd-b53e-1157a2c0b98a", "openfda": {"nui": ["N0000008486"], "upc": ["0370954488101"], "unii": ["563KS2PQY5"], "rxcui": ["993856"], "spl_set_id": ["68033c90-d9cc-4d5f-896c-9a61a0c3b529"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 mL in 1 BOTTLE, PLASTIC (70954-488-10)", "package_ndc": "70954-488-10", "marketing_start_date": "20220826"}], "brand_name": "Lacosamide", "product_id": "70954-488_8b5b4014-2795-4ebd-b53e-1157a2c0b98a", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70954-488", "dea_schedule": "CV", "generic_name": "Lacosamide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lacosamide", "active_ingredients": [{"name": "LACOSAMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA216151", "marketing_category": "ANDA", "marketing_start_date": "20220826", "listing_expiration_date": "20261231"}