Package 68001-114-06

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 68001-114-06
Digits Only 6800111406
Product NDC 68001-114
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-114-06)

Marketing

Marketing Status
Marketed Since 2014-02-13
Brand levetiracetam
Generic levetiracetam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3244b556-1f56-2c07-e063-6394a90a4f52", "openfda": {"nui": ["N0000008486"], "upc": ["0368001114066", "0368001113069"], "unii": ["44YRR34555"], "rxcui": ["807832", "846378"], "spl_set_id": ["402b488c-1733-4bf7-a7a8-b60805b022c9"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-114-06)", "package_ndc": "68001-114-06", "marketing_start_date": "20140213"}], "brand_name": "Levetiracetam", "product_id": "68001-114_3244b556-1f56-2c07-e063-6394a90a4f52", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68001-114", "generic_name": "Levetiracetam", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA091399", "marketing_category": "ANDA", "marketing_start_date": "20140213", "listing_expiration_date": "20261231"}