Package 70518-0947-1

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 70518-0947-1
Digits Only 7051809471
Product NDC 70518-0947
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0947-1)

Marketing

Marketing Status
Marketed Since 2020-05-28
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": "4848a665-886a-8671-e063-6294a90a3aae", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288"], "spl_set_id": ["1f4a0acc-d5f5-438d-96a0-897dfebdf6e4"], "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 (70518-0947-1)", "package_ndc": "70518-0947-1", "marketing_start_date": "20200528"}], "brand_name": "Levetiracetam", "product_id": "70518-0947_4848a665-886a-8671-e063-6294a90a3aae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-0947", "generic_name": "Levetiracetam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "250 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20180110", "listing_expiration_date": "20271231"}