Package 72189-510-60

Brand: levetiracetam er

Generic: levetiracetam er
NDC Package

Package Facts

Identity

Package NDC 72189-510-60
Digits Only 7218951060
Product NDC 72189-510
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-510-60)

Marketing

Marketing Status
Marketed Since 2023-08-25
Brand levetiracetam er
Generic levetiracetam er
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e5941-7089-8be7-e063-6394a90a92e3", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832"], "spl_set_id": ["03c449a1-9b40-a7da-e063-6394a90a984e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-510-60)", "package_ndc": "72189-510-60", "marketing_start_date": "20230825"}], "brand_name": "Levetiracetam ER", "product_id": "72189-510_2c4e5941-7089-8be7-e063-6394a90a92e3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72189-510", "generic_name": "Levetiracetam ER", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam ER", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA203468", "marketing_category": "ANDA", "marketing_start_date": "20230825", "listing_expiration_date": "20261231"}