Package 51672-4141-3

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 51672-4141-3
Digits Only 5167241413
Product NDC 51672-4141
Description

1000 TABLET, FILM COATED in 1 BOTTLE (51672-4141-3)

Marketing

Marketing Status
Marketed Since 2010-02-01
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": "559a39a2-ec8e-443b-9df0-4c909633981c", "openfda": {"nui": ["N0000008486"], "upc": ["0351672414160"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003", "403884"], "spl_set_id": ["bf412e94-ca36-4da9-83d7-fb0f1323cf21"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (51672-4141-0)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "51672-4141-0", "marketing_start_date": "20100201"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (51672-4141-1)", "package_ndc": "51672-4141-1", "marketing_start_date": "20100201"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (51672-4141-3)", "package_ndc": "51672-4141-3", "marketing_start_date": "20100201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51672-4141-6)", "package_ndc": "51672-4141-6", "marketing_start_date": "20100201"}], "brand_name": "Levetiracetam", "product_id": "51672-4141_559a39a2-ec8e-443b-9df0-4c909633981c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51672-4141", "generic_name": "Levetiracetam", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "250 mg/1"}], "application_number": "ANDA078960", "marketing_category": "ANDA", "marketing_start_date": "20100201", "listing_expiration_date": "20261231"}