levetiracetam

Generic: levetiracetam

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2337
Product ID 71335-2337_abdc51be-118f-4829-900f-f005efedbf7c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078993
Marketing Start 2009-01-15
Marketing End 2026-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713352337
Hyphenated Format 71335-2337

Supplemental Identifiers

RxCUI
311289
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 ANDA078993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-2337-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-2337-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-2337-3)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-2337-4)
  • 28 TABLET, FILM COATED in 1 BOTTLE (71335-2337-5)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-2337-6)
  • 21 TABLET, FILM COATED in 1 BOTTLE (71335-2337-7)
source: ndc

Packages (7)

71335-2337-1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2337-1) 71335-2337-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-2337-2) 71335-2337-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-2337-3) 71335-2337-4 120 TABLET, FILM COATED in 1 BOTTLE (71335-2337-4) 71335-2337-5 28 TABLET, FILM COATED in 1 BOTTLE (71335-2337-5) 71335-2337-6 100 TABLET, FILM COATED in 1 BOTTLE (71335-2337-6) 71335-2337-7 21 TABLET, FILM COATED in 1 BOTTLE (71335-2337-7)

Ingredients (1)

levetiracetam (500 mg/1)

Linked Drug Pages (1)

Levetiracetam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "abdc51be-118f-4829-900f-f005efedbf7c", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["23e2d43d-0578-4a78-925a-84389842d2db"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2337-1)", "package_ndc": "71335-2337-1", "marketing_end_date": "20260331", "marketing_start_date": "20240130"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2337-2)", "package_ndc": "71335-2337-2", "marketing_end_date": "20260331", "marketing_start_date": "20240716"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2337-3)", "package_ndc": "71335-2337-3", "marketing_end_date": "20260331", "marketing_start_date": "20240221"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2337-4)", "package_ndc": "71335-2337-4", "marketing_end_date": "20260331", "marketing_start_date": "20240716"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (71335-2337-5)", "package_ndc": "71335-2337-5", "marketing_end_date": "20260331", "marketing_start_date": "20240716"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-2337-6)", "package_ndc": "71335-2337-6", "marketing_end_date": "20260331", "marketing_start_date": "20240716"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (71335-2337-7)", "package_ndc": "71335-2337-7", "marketing_end_date": "20260331", "marketing_start_date": "20240716"}], "brand_name": "Levetiracetam", "product_id": "71335-2337_abdc51be-118f-4829-900f-f005efedbf7c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2337", "generic_name": "Levetiracetam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078993", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20090115"}