Package 71335-2282-1

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 71335-2282-1
Digits Only 7133522821
Product NDC 71335-2282
Product ID 71335-2282_0d94c381-f292-4e64-bc51-9b41504175c5
Description

500 TABLET in 1 BOTTLE (71335-2282-1)

Marketing

Marketing Status
Marketed Since 2024-08-12
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": "0d94c381-f292-4e64-bc51-9b41504175c5", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["b738377c-035e-4b2e-9909-0a8fe07aa0fb"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2282-1)", "package_ndc": "71335-2282-1", "marketing_start_date": "20240812"}], "brand_name": "Levetiracetam", "product_id": "71335-2282_0d94c381-f292-4e64-bc51-9b41504175c5", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2282", "generic_name": "Levetiracetam", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078858", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}