Package 51079-821-20

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 51079-821-20
Digits Only 5107982120
Product NDC 51079-821
Description

100 BLISTER PACK in 1 CARTON (51079-821-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-821-01)

Marketing

Marketing Status
Marketed Since 2008-11-04
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": "4369847b-77af-cd07-e063-6394a90a9251", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["08e1bfea-7f3f-42d9-823d-f75080e664ff"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (51079-821-20)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-821-01)", "package_ndc": "51079-821-20", "marketing_start_date": "20081104"}], "brand_name": "Levetiracetam", "product_id": "51079-821_4369847b-77af-cd07-e063-6394a90a9251", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51079-821", "generic_name": "levetiracetam", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA076919", "marketing_category": "ANDA", "marketing_start_date": "20081104", "listing_expiration_date": "20261231"}