Package 70518-1108-0

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 70518-1108-0
Digits Only 7051811080
Product NDC 70518-1108
Product ID 70518-1108_4859ece2-8153-78ce-e063-6294a90a4996
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1108-0)

Marketing

Marketing Status
Marketed Since 2018-04-11
Brand levetiracetam
Generic levetiracetam
Sample Package No

Linked Drug Pages (1)

Levetiracetam ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4859ece2-8153-78ce-e063-6294a90a4996", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["1c26c0ad-9d37-45c5-9091-849509f4fc01"], "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 in 1 BLISTER PACK (70518-1108-0)", "package_ndc": "70518-1108-0", "marketing_start_date": "20180411"}], "brand_name": "Levetiracetam", "product_id": "70518-1108_4859ece2-8153-78ce-e063-6294a90a4996", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-1108", "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": "ANDA078154", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20271231"}