Package 43063-499-60

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 43063-499-60
Digits Only 4306349960
Product NDC 43063-499
Description

60 TABLET in 1 BOTTLE, PLASTIC (43063-499-60)

Marketing

Marketing Status
Marketed Since 2012-02-09
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": "2f364228-05e4-2e79-e063-6294a90ac493", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["c2177034-e164-453c-be02-1cf91ce27a07"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (43063-499-60)", "package_ndc": "43063-499-60", "marketing_start_date": "20120209"}], "brand_name": "Levetiracetam", "product_id": "43063-499_2f364228-05e4-2e79-e063-6294a90ac493", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "43063-499", "generic_name": "Levetiracetam", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}