Package 80425-0443-1

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 80425-0443-1
Digits Only 8042504431
Product NDC 80425-0443
Description

7 TABLET, FILM COATED in 1 BOTTLE (80425-0443-1)

Marketing

Marketing Status
Marketed Since 2024-10-15
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": "248a470e-c977-fb5c-e063-6394a90abb66", "openfda": {"nui": ["N0000175599", "N0000020026"], "unii": ["742SXX0ICT"], "rxcui": ["402019"], "spl_set_id": ["248a4705-1403-e94a-e063-6294a90a3544"], "pharm_class_epc": ["Phosphodiesterase 5 Inhibitor [EPC]"], "pharm_class_moa": ["Phosphodiesterase 5 Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET, FILM COATED in 1 BOTTLE (80425-0443-1)", "package_ndc": "80425-0443-1", "marketing_start_date": "20241015"}], "brand_name": "Tadalafil", "product_id": "80425-0443_248a470e-c977-fb5c-e063-6394a90abb66", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "80425-0443", "generic_name": "Tadalafil", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "20 mg/1"}], "application_number": "ANDA210420", "marketing_category": "ANDA", "marketing_start_date": "20241015", "listing_expiration_date": "20261231"}