Package 69339-179-03

Brand: armodafinil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 69339-179-03
Digits Only 6933917903
Product NDC 69339-179
Description

30 TABLET in 1 BOTTLE (69339-179-03)

Marketing

Marketing Status
Marketed Since 2023-03-23
Brand armodafinil
Generic armodafinil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d93dca81-a0da-49ee-be61-86e713ab56cd", "openfda": {"upc": ["0369339177105", "0369339180051", "0369339178102", "0369339178034", "0369339180037", "0369339179031"], "unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["de2f0921-e791-426c-9192-2b7162e2158c"], "manufacturer_name": ["Natco Pharma USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (69339-179-03)", "package_ndc": "69339-179-03", "marketing_start_date": "20230323"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69339-179-10)", "package_ndc": "69339-179-10", "marketing_start_date": "20230323"}], "brand_name": "Armodafinil", "product_id": "69339-179_d93dca81-a0da-49ee-be61-86e713ab56cd", "dosage_form": "TABLET", "product_ndc": "69339-179", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Natco Pharma USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "ANDA202768", "marketing_category": "ANDA", "marketing_start_date": "20230323", "listing_expiration_date": "20261231"}