Package 67877-769-12

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 67877-769-12
Digits Only 6787776912
Product NDC 67877-769
Description

120 TABLET, FILM COATED in 1 BOTTLE (67877-769-12)

Marketing

Marketing Status
Marketed Since 2022-05-28
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": "40d1180e-73b5-4e73-8d42-15b99313496f", "openfda": {"nui": ["N0000008486"], "upc": ["0367877771601", "0367877769127", "0367877771335", "0367877768304", "0367877770055"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["591dd9f1-3681-4b2f-b096-7536826e3648"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (67877-769-05)", "package_ndc": "67877-769-05", "marketing_start_date": "20220528"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (67877-769-12)", "package_ndc": "67877-769-12", "marketing_start_date": "20220528"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67877-769-30)", "package_ndc": "67877-769-30", "marketing_start_date": "20220528"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (67877-769-33)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-769-33", "marketing_start_date": "20220528"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-769-38)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "67877-769-38", "marketing_start_date": "20241029"}], "brand_name": "Levetiracetam", "product_id": "67877-769_40d1180e-73b5-4e73-8d42-15b99313496f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "67877-769", "generic_name": "Levetiracetam", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA216375", "marketing_category": "ANDA", "marketing_start_date": "20220528", "listing_expiration_date": "20261231"}