levetiracetam

Generic: levetiracetam

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler direct rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 500 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-229
Product ID 72189-229_4c4bd407-ac66-f594-e063-6294a90a31fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090515
Listing Expiration 2027-12-31
Marketing Start 2021-06-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189229
Hyphenated Format 72189-229

Supplemental Identifiers

RxCUI
311288 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 ANDA090515 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (72189-229-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-229-90)
source: ndc

Packages (2)

72189-229-60 60 TABLET, FILM COATED in 1 BOTTLE (72189-229-60) 72189-229-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-229-90)

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": "4c4bd407-ac66-f594-e063-6294a90a31fe", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289"], "spl_set_id": ["c3b62114-a590-f4db-e053-2995a90a9d30"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72189-229-60)", "package_ndc": "72189-229-60", "marketing_start_date": "20210601"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-229-90)", "package_ndc": "72189-229-90", "marketing_start_date": "20210601"}], "brand_name": "LEVETIRACETAM", "product_id": "72189-229_4c4bd407-ac66-f594-e063-6294a90a31fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-229", "generic_name": "LEVETIRACETAM", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20210601", "listing_expiration_date": "20271231"}