Package 0093-3094-56

Brand: armodafinil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 0093-3094-56
Digits Only 0093309456
Product NDC 0093-3094
Product ID 0093-3094_ca66f83d-4d17-4516-9163-abdb19872555
Description

30 TABLET in 1 BOTTLE (0093-3094-56)

Marketing

Marketing Status
Discontinued 2028-05-31
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": "ca66f83d-4d17-4516-9163-abdb19872555", "openfda": {"upc": ["0300933093569", "0300933094566", "0300933090568"], "unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863", "861960"], "spl_set_id": ["b3cac300-c3d2-4189-a410-2aaf3773c090"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (0093-3094-56)", "package_ndc": "0093-3094-56", "marketing_end_date": "20280531", "marketing_start_date": "20161129"}], "brand_name": "Armodafinil", "product_id": "0093-3094_ca66f83d-4d17-4516-9163-abdb19872555", "dosage_form": "TABLET", "product_ndc": "0093-3094", "dea_schedule": "CIV", "generic_name": "Armodafinil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "250 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20280531", "marketing_start_date": "20161129"}