Package 0378-5619-91

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 0378-5619-91
Digits Only 0378561991
Product NDC 0378-5619
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5619-91)

Marketing

Marketing Status
Marketed Since 2009-12-10
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": "8eaa3318-fe96-4d3e-9f49-3286cb04bfbf", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289", "311290", "387003"], "spl_set_id": ["0a987d59-560f-4650-96ec-31aec81953b5"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5619-91)", "package_ndc": "0378-5619-91", "marketing_start_date": "20091210"}], "brand_name": "Levetiracetam", "product_id": "0378-5619_8eaa3318-fe96-4d3e-9f49-3286cb04bfbf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0378-5619", "generic_name": "levetiracetam", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA090261", "marketing_category": "ANDA", "marketing_start_date": "20091210", "listing_expiration_date": "20261231"}