Package 71335-1620-3
Brand: tadalafil
Generic: tadalafilPackage Facts
Identity
Package NDC
71335-1620-3
Digits Only
7133516203
Product NDC
71335-1620
Description
60 TABLET, FILM COATED in 1 BOTTLE (71335-1620-3)
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": "6120b19b-4b8b-42f8-9677-f2da2999d8ff", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["484814"], "spl_set_id": ["f8def23c-55ea-4796-9735-dbcb25104835"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1620-1)", "package_ndc": "71335-1620-1", "marketing_start_date": "20200624"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-1620-2)", "package_ndc": "71335-1620-2", "marketing_start_date": "20200820"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1620-3)", "package_ndc": "71335-1620-3", "marketing_start_date": "20210113"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1620-4)", "package_ndc": "71335-1620-4", "marketing_start_date": "20200603"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1620-5)", "package_ndc": "71335-1620-5", "marketing_start_date": "20241031"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71335-1620-6)", "package_ndc": "71335-1620-6", "marketing_start_date": "20241031"}], "brand_name": "Tadalafil", "product_id": "71335-1620_6120b19b-4b8b-42f8-9677-f2da2999d8ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-1620", "generic_name": "Tadalafil", "labeler_name": "Bryant Ranch Prepack", "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"}