levetiracetam

Generic: levetiracetam

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-360
Product ID 63187-360_e47bfa3c-961e-45d8-a06a-d2d2a91fe115
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078154
Listing Expiration 2026-12-31
Marketing Start 2009-01-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187360
Hyphenated Format 63187-360

Supplemental Identifiers

RxCUI
311289
UPC
0363187360603
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 ANDA078154 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (63187-360-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (63187-360-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (63187-360-90)
source: ndc

Packages (3)

Ingredients (1)

levetiracetam (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e47bfa3c-961e-45d8-a06a-d2d2a91fe115", "openfda": {"nui": ["N0000008486"], "upc": ["0363187360603"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["6bdbc193-d86b-4bd5-8e88-4ea964d2cdde"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-360-30)", "package_ndc": "63187-360-30", "marketing_start_date": "20160801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-360-60)", "package_ndc": "63187-360-60", "marketing_start_date": "20160801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-360-90)", "package_ndc": "63187-360-90", "marketing_start_date": "20160801"}], "brand_name": "Levetiracetam", "product_id": "63187-360_e47bfa3c-961e-45d8-a06a-d2d2a91fe115", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63187-360", "generic_name": "Levetiracetam", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078154", "marketing_category": "ANDA", "marketing_start_date": "20090101", "listing_expiration_date": "20261231"}