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 50090-7820
Product ID 50090-7820_184de745-659c-4ddd-929a-4edc68912baf
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 500907820
Hyphenated Format 50090-7820

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 (50090-7820-0)
  • 500 TABLET in 1 BOTTLE (50090-7820-1)
source: ndc

Packages (2)

50090-7820-0 120 TABLET in 1 BOTTLE (50090-7820-0) 50090-7820-1 500 TABLET in 1 BOTTLE (50090-7820-1)

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": "184de745-659c-4ddd-929a-4edc68912baf", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["deca634a-651e-4c70-9fc3-b0087b537b0a"], "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 (50090-7820-0)", "package_ndc": "50090-7820-0", "marketing_start_date": "20251211"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50090-7820-1)", "package_ndc": "50090-7820-1", "marketing_start_date": "20251211"}], "brand_name": "Levetiracetam", "product_id": "50090-7820_184de745-659c-4ddd-929a-4edc68912baf", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7820", "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"}