Package 0378-3433-93

Brand: armodafinil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 0378-3433-93
Digits Only 0378343393
Product NDC 0378-3433
Description

30 TABLET in 1 BOTTLE, PLASTIC (0378-3433-93)

Marketing

Marketing Status
Marketed Since 2016-06-01
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": "34fcca9f-37ba-40d9-9032-6ffeeb031a36", "openfda": {"upc": ["0303783433936", "0303783431932", "0303783432939"], "unii": ["V63XWA605I"], "rxcui": ["724859", "724861", "724863"], "spl_set_id": ["de0799f7-7644-4057-a7da-75436f978c61"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (0378-3433-93)", "package_ndc": "0378-3433-93", "marketing_start_date": "20160601"}], "brand_name": "Armodafinil", "product_id": "0378-3433_34fcca9f-37ba-40d9-9032-6ffeeb031a36", "dosage_form": "TABLET", "product_ndc": "0378-3433", "dea_schedule": "CIV", "generic_name": "armodafinil", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Armodafinil", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "250 mg/1"}], "application_number": "ANDA200043", "marketing_category": "ANDA", "marketing_start_date": "20160601", "listing_expiration_date": "20261231"}