Package 63459-220-30

Brand: nuvigil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 63459-220-30
Digits Only 6345922030
Product NDC 63459-220
Product ID 63459-220_a70488d7-57ea-446e-89c2-87b0ecc90023
Description

30 TABLET in 1 BOTTLE (63459-220-30)

Marketing

Marketing Status
Discontinued 2026-03-31
Brand nuvigil
Generic armodafinil
Sample Package No

Linked Drug Pages (1)

Nuvigil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a70488d7-57ea-446e-89c2-87b0ecc90023", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "805659", "805661", "805663", "861960", "861962"], "spl_set_id": ["d878aed0-ddbf-8fa1-abf7-d3e480260845"], "manufacturer_name": ["Cephalon, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63459-220-30)", "package_ndc": "63459-220-30", "marketing_end_date": "20260331", "marketing_start_date": "20140220"}], "brand_name": "Nuvigil", "product_id": "63459-220_a70488d7-57ea-446e-89c2-87b0ecc90023", "dosage_form": "TABLET", "product_ndc": "63459-220", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nuvigil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA", "marketing_end_date": "20260331", "marketing_start_date": "20140220"}