Package 0781-8037-31

Brand: armodafinil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 0781-8037-31
Digits Only 0781803731
Product NDC 0781-8037
Product ID 0781-8037_dea0ad34-a35f-42ba-a6b6-dea58a16868f
Description

30 TABLET in 1 BOTTLE (0781-8037-31)

Marketing

Marketing Status
Discontinued 2028-06-30
Brand armodafinil
Generic armodafinil
Sample Package No

Linked Drug Pages (1)

Armodafinil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dea0ad34-a35f-42ba-a6b6-dea58a16868f", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["a3341ec8-1ad4-49e2-922b-13d1b30c8c1d"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0781-8037-31)", "package_ndc": "0781-8037-31", "marketing_end_date": "20280630", "marketing_start_date": "20161201"}], "brand_name": "Armodafinil", "product_id": "0781-8037_dea0ad34-a35f-42ba-a6b6-dea58a16868f", "dosage_form": "TABLET", "product_ndc": "0781-8037", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "150 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20280630", "marketing_start_date": "20161201"}