Package 60505-4849-3

Brand: nuvigil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 60505-4849-3
Digits Only 6050548493
Product NDC 60505-4849
Product ID 60505-4849_ab761afd-b864-a5f9-e204-952c98103e63
Description

30 TABLET in 1 BOTTLE (60505-4849-3)

Marketing

Marketing Status
Marketed Since 2025-08-31
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": "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 (60505-4849-3)", "package_ndc": "60505-4849-3", "marketing_start_date": "20250831"}], "brand_name": "Nuvigil", "product_id": "60505-4849_ab761afd-b864-a5f9-e204-952c98103e63", "dosage_form": "TABLET", "product_ndc": "60505-4849", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nuvigil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA", "marketing_start_date": "20250831", "listing_expiration_date": "20261231"}