Package 72162-2236-3

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2236-3
Digits Only 7216222363
Product NDC 72162-2236
Product ID 72162-2236_891c56c9-912d-4e77-8649-c130c93424d3
Description

30 TABLET in 1 BOTTLE (72162-2236-3)

Marketing

Marketing Status
Marketed Since 2024-09-06
Brand vardenafil hydrochloride
Generic vardenafil hydrochloride
Sample Package No

Linked Drug Pages (1)

Vardenafil Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "891c56c9-912d-4e77-8649-c130c93424d3", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349480"], "spl_set_id": ["083a3282-254f-4042-b0eb-70f76a279f10"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2236-3)", "package_ndc": "72162-2236-3", "marketing_start_date": "20240906"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "72162-2236_891c56c9-912d-4e77-8649-c130c93424d3", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72162-2236", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}