Package 71205-720-04
Brand: tadalafil
Generic: tadalafilPackage Facts
Identity
Package NDC
71205-720-04
Digits Only
7120572004
Product NDC
71205-720
Description
4 TABLET, FILM COATED in 1 BOTTLE (71205-720-04)
Marketing
Marketing Status
Brand
tadalafil
Generic
tadalafil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7a105ef9-7129-4ce1-bd8d-ae316bf348e2", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["484814"], "spl_set_id": ["7a105ef9-7129-4ce1-bd8d-ae316bf348e2"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (71205-720-04)", "package_ndc": "71205-720-04", "marketing_start_date": "20221116"}], "brand_name": "Tadalafil", "product_id": "71205-720_7a105ef9-7129-4ce1-bd8d-ae316bf348e2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71205-720", "generic_name": "Tadalafil", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "10 mg/1"}], "application_number": "ANDA209167", "marketing_category": "ANDA", "marketing_start_date": "20200403", "listing_expiration_date": "20261231"}