nuvigil

Generic: armodafinil

Labeler: apotex corp.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name nuvigil
Generic Name armodafinil
Labeler apotex corp.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

armodafinil 150 mg/1

Manufacturer
Apotex Corp.

Identifiers & Regulatory

Product NDC 60505-4847
Product ID 60505-4847_ab761afd-b864-a5f9-e204-952c98103e63
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021875
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2025-08-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 605054847
Hyphenated Format 60505-4847

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
  • 150 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (60505-4847-3)
source: ndc

Packages (1)

60505-4847-3 30 TABLET in 1 BOTTLE (60505-4847-3)

Ingredients (1)

armodafinil (150 mg/1)

Linked Drug Pages (1)

Nuvigil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ab761afd-b864-a5f9-e204-952c98103e63", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "805659", "805661", "805663", "861960", "861962"], "spl_set_id": ["a69631d0-1263-769e-b232-4ab9160e0fa3"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (60505-4847-3)", "package_ndc": "60505-4847-3", "marketing_start_date": "20250831"}], "brand_name": "Nuvigil", "product_id": "60505-4847_ab761afd-b864-a5f9-e204-952c98103e63", "dosage_form": "TABLET", "product_ndc": "60505-4847", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nuvigil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "150 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA", "marketing_start_date": "20250831", "listing_expiration_date": "20261231"}