Package 69102-106-01
Brand: levetiracetam
Generic: levetiracetamPackage Facts
Identity
Package NDC
69102-106-01
Digits Only
6910210601
Product NDC
69102-106
Description
120 TABLET in 1 BOTTLE (69102-106-01)
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": "c7262ce0-c186-487b-9808-b340d31d8fe4", "openfda": {"nui": ["N0000008486"], "upc": ["0369102107018", "0369102106011"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003", "1875868"], "spl_set_id": ["e662bf5b-c81c-4bcd-ba2e-552df95ca6f9"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["OWP Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (69102-106-01)", "package_ndc": "69102-106-01", "marketing_start_date": "20201028"}], "brand_name": "Levetiracetam", "product_id": "69102-106_c7262ce0-c186-487b-9808-b340d31d8fe4", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "69102-106", "generic_name": "Levetiracetam", "labeler_name": "OWP Pharmaceuticals, Inc.", "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": "20201028", "listing_expiration_date": "20261231"}