Package 71335-2357-1

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2357-1
Digits Only 7133523571
Product NDC 71335-2357
Product ID 71335-2357_d372a596-aa3a-4bd7-b311-ee32b051d758
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2357-1)

Marketing

Marketing Status
Marketed Since 2024-05-28
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": "d372a596-aa3a-4bd7-b311-ee32b051d758", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349480"], "spl_set_id": ["d8a5cc4b-9d9d-43af-9ee4-57381aa6368a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2357-1)", "package_ndc": "71335-2357-1", "marketing_start_date": "20240528"}], "brand_name": "VARDENAFIL HYDROCHLORIDE", "product_id": "71335-2357_d372a596-aa3a-4bd7-b311-ee32b051d758", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-2357", "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": "ANDA214031", "marketing_category": "ANDA", "marketing_start_date": "20200805", "listing_expiration_date": "20261231"}