Package 72789-152-60

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 72789-152-60
Digits Only 7278915260
Product NDC 72789-152
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-152-60)

Marketing

Marketing Status
Marketed Since 2020-12-31
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": "40a76631-dac1-b888-e063-6394a90a19f9", "openfda": {"nui": ["N0000008486"], "upc": ["0372789152608"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["792db8dc-177b-4864-8600-12823819082d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-152-60)", "package_ndc": "72789-152-60", "marketing_start_date": "20201231"}], "brand_name": "Levetiracetam", "product_id": "72789-152_40a76631-dac1-b888-e063-6394a90a19f9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-152", "generic_name": "Levetiracetam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}