Package 72189-133-30
Brand: armodafinil
Generic: armodafinilPackage Facts
Identity
Package NDC
72189-133-30
Digits Only
7218913330
Product NDC
72189-133
Description
30 TABLET in 1 BOTTLE (72189-133-30)
Marketing
Marketing Status
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": "2c28fdcb-8329-f51c-e063-6394a90a2fe2", "openfda": {"unii": ["V63XWA605I"], "rxcui": ["724861"], "spl_set_id": ["b1ba1cdd-cf57-7a8c-e053-2a95a90a2c19"], "manufacturer_name": ["direct rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-133-30)", "package_ndc": "72189-133-30", "marketing_start_date": "20201015"}], "brand_name": "ARMODAFINIL", "product_id": "72189-133_2c28fdcb-8329-f51c-e063-6394a90a2fe2", "dosage_form": "TABLET", "product_ndc": "72189-133", "dea_schedule": "CIV", "generic_name": "ARMODAFINIL", "labeler_name": "direct rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARMODAFINIL", "active_ingredients": [{"name": "ARMODAFINIL", "strength": "250 mg/1"}], "application_number": "ANDA206069", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}