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
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-9757
Product ID 71335-9757_39df4d1a-2fb2-4e2b-90ac-de1d53aaf99e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091491
Listing Expiration 2026-12-31
Marketing Start 2023-05-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713359757
Hyphenated Format 71335-9757

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 ANDA091491 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-9757-1)
  • 60 TABLET in 1 BOTTLE (71335-9757-2)
  • 30 TABLET in 1 BOTTLE (71335-9757-3)
  • 120 TABLET in 1 BOTTLE (71335-9757-4)
  • 28 TABLET in 1 BOTTLE (71335-9757-5)
  • 100 TABLET in 1 BOTTLE (71335-9757-6)
  • 21 TABLET in 1 BOTTLE (71335-9757-7)
source: ndc

Packages (7)

Ingredients (1)

levetiracetam (500 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39df4d1a-2fb2-4e2b-90ac-de1d53aaf99e", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["7696961e-dfff-422a-b72f-e31ceeac10af"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9757-1)", "package_ndc": "71335-9757-1", "marketing_start_date": "20240530"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9757-2)", "package_ndc": "71335-9757-2", "marketing_start_date": "20230927"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9757-3)", "package_ndc": "71335-9757-3", "marketing_start_date": "20240522"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9757-4)", "package_ndc": "71335-9757-4", "marketing_start_date": "20240530"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-9757-5)", "package_ndc": "71335-9757-5", "marketing_start_date": "20231208"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-9757-6)", "package_ndc": "71335-9757-6", "marketing_start_date": "20240530"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-9757-7)", "package_ndc": "71335-9757-7", "marketing_start_date": "20240530"}], "brand_name": "Levetiracetam", "product_id": "71335-9757_39df4d1a-2fb2-4e2b-90ac-de1d53aaf99e", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-9757", "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": "ANDA091491", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}