Package 70518-4301-0

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 70518-4301-0
Digits Only 7051843010
Product NDC 70518-4301
Description

30 TABLET in 1 BLISTER PACK (70518-4301-0)

Marketing

Marketing Status
Marketed Since 2025-03-04
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": "3b4d042e-fbc7-b2b5-e063-6394a90af744", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["c12d8af3-39a8-4690-8d47-43dec70b7579"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4301-0)", "package_ndc": "70518-4301-0", "marketing_start_date": "20250304"}], "brand_name": "Levetiracetam", "product_id": "70518-4301_3b4d042e-fbc7-b2b5-e063-6394a90af744", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4301", "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": "ANDA091491", "marketing_category": "ANDA", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}