levetiracetam

Generic: levetiracetam

Labeler: coupler llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler coupler llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 750 mg/1

Manufacturer
Coupler LLC

Identifiers & Regulatory

Product NDC 67046-1615
Product ID 67046-1615_43df447e-dc5b-dc8f-e063-6294a90a8f9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215069
Listing Expiration 2026-12-31
Marketing Start 2025-11-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 670461615
Hyphenated Format 67046-1615

Supplemental Identifiers

RxCUI
311290
UNII
44YRR34555
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 levetiracetam (source: ndc)
Generic Name levetiracetam (source: ndc)
Application Number ANDA215069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1615-3)
source: ndc

Packages (1)

Ingredients (1)

levetiracetam (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "43df447e-dc5b-dc8f-e063-6294a90a8f9f", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311290"], "spl_set_id": ["43df4156-0958-e496-e063-6294a90a5329"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1615-3)", "package_ndc": "67046-1615-3", "marketing_start_date": "20251118"}], "brand_name": "Levetiracetam", "product_id": "67046-1615_43df447e-dc5b-dc8f-e063-6294a90a8f9f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67046-1615", "generic_name": "Levetiracetam", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA215069", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}