Package 50090-7315-0

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 50090-7315-0
Digits Only 5009073150
Product NDC 50090-7315
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7315-0)

Marketing

Marketing Status
Marketed Since 2024-10-14
Brand tadalafil
Generic tadalafil
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e7caaf8f-10ff-4637-82e0-d152f4029bce", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["403957"], "spl_set_id": ["00cbc656-768d-4995-bb6d-a0d4b32a248c"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7315-0)", "package_ndc": "50090-7315-0", "marketing_start_date": "20241014"}], "brand_name": "tadalafil", "product_id": "50090-7315_e7caaf8f-10ff-4637-82e0-d152f4029bce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-7315", "generic_name": "Tadalafil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "5 mg/1"}], "application_number": "ANDA215556", "marketing_category": "ANDA", "marketing_start_date": "20230401", "listing_expiration_date": "20261231"}