Package 70518-1901-1

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 70518-1901-1
Digits Only 7051819011
Product NDC 70518-1901
Description

30 POUCH in 1 BOX (70518-1901-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1901-2)

Marketing

Marketing Status
Marketed Since 2021-08-04
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": "4987ad82-cd46-45b0-e063-6394a90af127", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["387003"], "spl_set_id": ["ae405796-1eca-4890-bcb2-e1b07654a24d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 BOX (70518-1901-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-1901-2)", "package_ndc": "70518-1901-1", "marketing_start_date": "20210804"}], "brand_name": "Levetiracetam", "product_id": "70518-1901_4987ad82-cd46-45b0-e063-6394a90af127", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-1901", "generic_name": "Levetiracetam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20190222", "listing_expiration_date": "20271231"}