Package 0480-2309-56

Brand: tadalafil

Generic: tadalafil
NDC Package

Package Facts

Identity

Package NDC 0480-2309-56
Digits Only 0480230956
Product NDC 0480-2309
Product ID 0480-2309_84ad5d1f-f226-4562-a511-2046f388d2a1
Description

30 TABLET, FILM COATED in 1 BOTTLE (0480-2309-56)

Marketing

Marketing Status
Marketed Since 2024-01-16
Brand tadalafil
Generic tadalafil
Sample Package No

Linked Drug Pages (1)

Tadalafil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "84ad5d1f-f226-4562-a511-2046f388d2a1", "openfda": {}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0480-2309-56)", "package_ndc": "0480-2309-56", "marketing_start_date": "20240116"}], "brand_name": "Tadalafil", "product_id": "0480-2309_84ad5d1f-f226-4562-a511-2046f388d2a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0480-2309", "generic_name": "Tadalafil", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tadalafil", "active_ingredients": [{"name": "TADALAFIL", "strength": "5 mg/1"}], "application_number": "ANDA205885", "marketing_category": "ANDA", "marketing_start_date": "20240116", "listing_expiration_date": "20271231"}