Package 13668-016-12

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 13668-016-12
Digits Only 1366801612
Product NDC 13668-016
Product ID 13668-016_b8792837-f86a-4e67-b1a5-ec8ca278fe77
Description

120 TABLET in 1 BOTTLE (13668-016-12)

Marketing

Marketing Status
Marketed Since 2009-01-15
Brand levetiracetam
Generic levetiracetam
Sample Package No

Linked Drug Pages (1)

Levetiracetam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b8792837-f86a-4e67-b1a5-ec8ca278fe77", "openfda": {"nui": ["N0000008486"], "upc": ["0313668017601", "0313668016604", "0313668014600", "0313668015607"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["6ab24168-058d-496e-9023-da8ee6353eb3"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (13668-016-05)", "package_ndc": "13668-016-05", "marketing_start_date": "20090115"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (13668-016-12)", "package_ndc": "13668-016-12", "marketing_start_date": "20090115"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (13668-016-25)", "package_ndc": "13668-016-25", "marketing_start_date": "20090115"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (13668-016-60)", "package_ndc": "13668-016-60", "marketing_start_date": "20090115"}, {"sample": false, "description": "800 TABLET in 1 BOTTLE (13668-016-67)", "package_ndc": "13668-016-67", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "13668-016_b8792837-f86a-4e67-b1a5-ec8ca278fe77", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "13668-016", "generic_name": "Levetiracetam", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA078858", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}