Package 70518-4125-0
Brand: levetiracetam er
Generic: levetiracetamPackage Facts
Identity
Package NDC
70518-4125-0
Digits Only
7051841250
Product NDC
70518-4125
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-4125-0)
Marketing
Marketing Status
Brand
levetiracetam er
Generic
levetiracetam
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c5503f0-b200-3733-e063-6394a90a0ec9", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832"], "spl_set_id": ["2d57f22f-fecc-466e-a444-87708c7c2f80"], "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 BLISTER PACK (70518-4125-0)", "package_ndc": "70518-4125-0", "marketing_start_date": "20240701"}], "brand_name": "Levetiracetam ER", "product_id": "70518-4125_3c5503f0-b200-3733-e063-6394a90a0ec9", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4125", "generic_name": "Levetiracetam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "brand_name_suffix": "ER", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA205130", "marketing_category": "ANDA", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}