Package 50474-599-66

Brand: keppra xr

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 50474-599-66
Digits Only 5047459966
Product NDC 50474-599
Product ID 50474-599_38534148-3717-03b3-e063-6394a90a0f1e
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-599-66)

Marketing

Marketing Status
Marketed Since 2009-04-01
Brand keppra xr
Generic levetiracetam
Sample Package No

Linked Drug Pages (1)

Keppra XR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38534148-3717-03b3-e063-6394a90a0f1e", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832", "807834", "846378", "847673"], "spl_set_id": ["2919e43b-69a8-434c-a2d2-1f3ecd7554c0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["UCB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50474-599-66)", "package_ndc": "50474-599-66", "marketing_start_date": "20090401"}], "brand_name": "Keppra XR", "product_id": "50474-599_38534148-3717-03b3-e063-6394a90a0f1e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50474-599", "generic_name": "levetiracetam", "labeler_name": "UCB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Keppra", "brand_name_suffix": "XR", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "NDA022285", "marketing_category": "NDA", "marketing_start_date": "20090401", "listing_expiration_date": "20261231"}