levetiracetam

Generic: levetiracetam

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7521
Product ID 50090-7521_48d58ab4-2d5c-4ac2-a2f3-a8b5163f0f28
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 500907521
Hyphenated Format 50090-7521

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
  • 120 TABLET in 1 BOTTLE (50090-7521-0)
  • 60 TABLET in 1 BOTTLE (50090-7521-1)
  • 90 TABLET in 1 BOTTLE (50090-7521-2)
  • 180 TABLET in 1 BOTTLE (50090-7521-3)
source: ndc

Packages (4)

50090-7521-0 120 TABLET in 1 BOTTLE (50090-7521-0) 50090-7521-1 60 TABLET in 1 BOTTLE (50090-7521-1) 50090-7521-2 90 TABLET in 1 BOTTLE (50090-7521-2) 50090-7521-3 180 TABLET in 1 BOTTLE (50090-7521-3)

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": "48d58ab4-2d5c-4ac2-a2f3-a8b5163f0f28", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["c82313cb-744f-45ef-b74c-1bdd055b2193"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (50090-7521-0)", "package_ndc": "50090-7521-0", "marketing_start_date": "20250317"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7521-1)", "package_ndc": "50090-7521-1", "marketing_start_date": "20250317"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7521-2)", "package_ndc": "50090-7521-2", "marketing_start_date": "20250317"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (50090-7521-3)", "package_ndc": "50090-7521-3", "marketing_start_date": "20250317"}], "brand_name": "Levetiracetam", "product_id": "50090-7521_48d58ab4-2d5c-4ac2-a2f3-a8b5163f0f28", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7521", "generic_name": "Levetiracetam", "labeler_name": "A-S Medication Solutions", "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"}