Package 70518-4005-1

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 70518-4005-1
Digits Only 7051840051
Product NDC 70518-4005
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4005-1)

Marketing

Marketing Status
Marketed Since 2025-03-25
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": "4c965546-7569-17cd-e063-6394a90aef59", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832"], "spl_set_id": ["9bdef24b-c50e-4e6a-8650-59d78009f472"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4005-1)", "package_ndc": "70518-4005-1", "marketing_start_date": "20250325"}], "brand_name": "LEVETIRACETAM", "product_id": "70518-4005_4c965546-7569-17cd-e063-6394a90aef59", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4005", "generic_name": "LEVETIRACETAM", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA203468", "marketing_category": "ANDA", "marketing_start_date": "20240131", "listing_expiration_date": "20271231"}