Package 0472-0235-16

Brand: levetiracetam

Generic: levetiracetam
NDC Package

Package Facts

Identity

Package NDC 0472-0235-16
Digits Only 0472023516
Product NDC 0472-0235
Description

473 mL in 1 BOTTLE, PLASTIC (0472-0235-16)

Marketing

Marketing Status
Marketed Since 2009-01-15
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": "b64ea04d-69cd-4d88-885a-4210492d881c", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["403884"], "spl_set_id": ["5cb4a1db-f32d-44af-8985-0a94ca506468"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE, PLASTIC (0472-0235-16)", "package_ndc": "0472-0235-16", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "0472-0235_b64ea04d-69cd-4d88-885a-4210492d881c", "dosage_form": "SOLUTION", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "0472-0235", "generic_name": "Levetiracetam", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "100 mg/mL"}], "application_number": "ANDA078976", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}