levetiracetam

Generic: levetiracetam

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name levetiracetam
Generic Name levetiracetam
Labeler american health packaging
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

levetiracetam 250 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-859
Product ID 68084-859_2737b5f9-5127-8b84-e063-6294a90aa140
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078993
Listing Expiration 2026-12-31
Marketing Start 2015-02-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084859
Hyphenated Format 68084-859

Supplemental Identifiers

RxCUI
311288 311290
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 ANDA078993 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-859-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-859-11)
source: ndc

Packages (1)

68084-859-01 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-859-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-859-11)

Ingredients (1)

levetiracetam (250 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": "2737b5f9-5127-8b84-e063-6294a90aa140", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288", "311290"], "spl_set_id": ["fc8bf57e-8aa2-4d3c-856d-b19de65e3ba0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-859-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-859-11)", "package_ndc": "68084-859-01", "marketing_start_date": "20150204"}], "brand_name": "Levetiracetam", "product_id": "68084-859_2737b5f9-5127-8b84-e063-6294a90aa140", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68084-859", "generic_name": "Levetiracetam", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "250 mg/1"}], "application_number": "ANDA078993", "marketing_category": "ANDA", "marketing_start_date": "20150204", "listing_expiration_date": "20261231"}