Package 76494-529-12
Brand: levetiracetam
Generic: levetiracetamPackage Facts
Identity
Package NDC
76494-529-12
Digits Only
7649452912
Product NDC
76494-529
Description
120 TABLET, FILM COATED in 1 BOTTLE (76494-529-12)
Marketing
Marketing Status
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": "bf716ab6-d438-4a19-8193-dbc05b4eabad", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["d818ef84-9b3e-434b-92d9-910cfa8af7da"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Prinston Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (76494-529-12)", "package_ndc": "76494-529-12", "marketing_start_date": "20120911"}], "brand_name": "Levetiracetam", "product_id": "76494-529_bf716ab6-d438-4a19-8193-dbc05b4eabad", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "76494-529", "generic_name": "Levetiracetam", "labeler_name": "Prinston Pharmaceutical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078106", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}