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, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 1000 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7333
Product ID 50090-7333_e912f362-a9eb-47aa-a9f5-261deee63d79
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215069
Listing Expiration 2026-12-31
Marketing Start 2021-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907333
Hyphenated Format 50090-7333

Supplemental Identifiers

RxCUI
387003
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 ANDA215069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (50090-7333-1)
  • 180 TABLET, FILM COATED in 1 BOTTLE (50090-7333-2)
source: ndc

Packages (2)

50090-7333-1 60 TABLET, FILM COATED in 1 BOTTLE (50090-7333-1) 50090-7333-2 180 TABLET, FILM COATED in 1 BOTTLE (50090-7333-2)

Ingredients (1)

levetiracetam (1000 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": "e912f362-a9eb-47aa-a9f5-261deee63d79", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["387003"], "spl_set_id": ["8a8472dc-b97e-445d-bf51-b6e618cae1b6"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7333-1)", "package_ndc": "50090-7333-1", "marketing_start_date": "20241015"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-7333-2)", "package_ndc": "50090-7333-2", "marketing_start_date": "20241015"}], "brand_name": "Levetiracetam", "product_id": "50090-7333_e912f362-a9eb-47aa-a9f5-261deee63d79", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7333", "generic_name": "Levetiracetam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA215069", "marketing_category": "ANDA", "marketing_start_date": "20210611", "listing_expiration_date": "20261231"}