Package 68382-899-05
Brand: tadalafil
Generic: tadalafilPackage Facts
Identity
Package NDC
68382-899-05
Digits Only
6838289905
Product NDC
68382-899
Description
500 TABLET, FILM COATED in 1 BOTTLE (68382-899-05)
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": "5a958db7-5c0e-4cf0-9227-230886cf9bf8", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019", "403957", "484814", "757707"], "spl_set_id": ["cfe43ab8-8721-4db8-8810-f0072cf8f4d3"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68382-899-01)", "package_ndc": "68382-899-01", "marketing_start_date": "20190327"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68382-899-05)", "package_ndc": "68382-899-05", "marketing_start_date": "20190327"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68382-899-06)", "package_ndc": "68382-899-06", "marketing_start_date": "20190327"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (68382-899-10)", "package_ndc": "68382-899-10", "marketing_start_date": "20190327"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68382-899-16)", "package_ndc": "68382-899-16", "marketing_start_date": "20190327"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68382-899-99) / 15 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68382-899-99", "marketing_start_date": "20190327"}], "brand_name": "Tadalafil", "product_id": "68382-899_5a958db7-5c0e-4cf0-9227-230886cf9bf8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68382-899", "generic_name": "Tadalafil", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA206693", "marketing_category": "ANDA", "marketing_start_date": "20190327", "listing_expiration_date": "20261231"}