Package 51655-487-52
Brand: tadalafil
Generic: tadalafilPackage Facts
Identity
Package NDC
51655-487-52
Digits Only
5165548752
Product NDC
51655-487
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-487-52)
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": "490f748c-4026-e630-e063-6294a90ac547", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["403957"], "spl_set_id": ["f317fe1e-d7c4-fb8b-e053-2a95a90a5445"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-487-52)", "package_ndc": "51655-487-52", "marketing_start_date": "20201125"}], "brand_name": "Tadalafil", "product_id": "51655-487_490f748c-4026-e630-e063-6294a90ac547", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "51655-487", "generic_name": "Tadalafil", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "5 mg/1"}], "application_number": "ANDA209167", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20271231"}