Package 72189-353-30

Brand: armodafinil

Generic: armodafinil
NDC Package

Package Facts

Identity

Package NDC 72189-353-30
Digits Only 7218935330
Product NDC 72189-353
Product ID 72189-353_2c4c8cee-041f-c5ef-e063-6394a90a8cfd
Description

30 TABLET in 1 BOTTLE (72189-353-30)

Marketing

Marketing Status
Marketed Since 2022-04-29
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": "2c4c8cee-041f-c5ef-e063-6394a90a8cfd", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["861960"], "spl_set_id": ["ddd06dab-0855-5b4e-e053-2a95a90a5e67"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-353-30)", "package_ndc": "72189-353-30", "marketing_start_date": "20220429"}], "brand_name": "ARMODAFINIL", "product_id": "72189-353_2c4c8cee-041f-c5ef-e063-6394a90a8cfd", "dosage_form": "TABLET", "product_ndc": "72189-353", "dea_schedule": "CIV", "generic_name": "ARMODAFINIL", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARMODAFINIL", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "200 mg/1"}], "application_number": "NDA021875", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220429", "listing_expiration_date": "20261231"}