Package 16714-034-02

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 16714-034-02
Digits Only 1671403402
Product NDC 16714-034
Description

500 TABLET, FILM COATED in 1 BOTTLE (16714-034-02)

Marketing

Marketing Status
Marketed Since 2022-03-29
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": "40911071-2280-bd37-e063-6394a90a0156", "openfda": {"nui": ["N0000008486"], "upc": ["0316714034010", "0316714035024", "0316714034027", "0316714537016", "0316714310015", "0316714035017", "0316714537023"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["3884cb76-822b-400d-9b24-49c286c9b6f7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (16714-034-01)", "package_ndc": "16714-034-01", "marketing_start_date": "20220329"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16714-034-02)", "package_ndc": "16714-034-02", "marketing_start_date": "20220329"}], "brand_name": "Levetiracetam", "product_id": "16714-034_40911071-2280-bd37-e063-6394a90a0156", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "16714-034", "generic_name": "Levetiracetam", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "250 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20220329", "listing_expiration_date": "20261231"}