Package 51655-325-52

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 51655-325-52
Digits Only 5165532552
Product NDC 51655-325
Product ID 51655-325_48eb084e-5a5e-4843-e063-6294a90a7344
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-325-52)

Marketing

Marketing Status
Marketed Since 2023-05-19
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": "48eb084e-5a5e-4843-e063-6294a90a7344", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["fc4c72e2-9cba-88d9-e053-6394a90a0426"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-325-52)", "package_ndc": "51655-325-52", "marketing_start_date": "20230519"}], "brand_name": "Levetiracetam", "product_id": "51655-325_48eb084e-5a5e-4843-e063-6294a90a7344", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51655-325", "generic_name": "Levetiracetam", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20271231"}