nuvigil

Generic: armodafinil

Labeler: cephalon, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name nuvigil
Generic Name armodafinil
Labeler cephalon, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 250 mg/1

Manufacturer
Cephalon, LLC

Identifiers & Regulatory

Product NDC 63459-225
Product ID 63459-225_a70488d7-57ea-446e-89c2-87b0ecc90023
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021875
DEA Schedule civ
Marketing Start 2009-05-26
Marketing End 2026-06-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63459225
Hyphenated Format 63459-225

Supplemental Identifiers

RxCUI
724859 724861 724863 805659 805661 805663 861960 861962
UNII
V63XWA605I

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name nuvigil (source: ndc)
Generic Name armodafinil (source: ndc)
Application Number NDA021875 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63459-225-30)
source: ndc

Packages (1)

Ingredients (1)

armodafinil (250 mg/1)

Linked Drug Pages (1)

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 (63459-225-30)", "package_ndc": "63459-225-30", "marketing_end_date": "20260630", "marketing_start_date": "20110103"}], "brand_name": "Nuvigil", "product_id": "63459-225_a70488d7-57ea-446e-89c2-87b0ecc90023", "dosage_form": "TABLET", "product_ndc": "63459-225", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nuvigil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "250 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA", "marketing_end_date": "20260630", "marketing_start_date": "20090526"}