Package 71335-9696-1

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-9696-1
Digits Only 7133596961
Product NDC 71335-9696
Product ID 71335-9696_c4b53c3e-e0c7-4368-beda-8c27a32ad5c9
Description

30 TABLET in 1 BOTTLE (71335-9696-1)

Marketing

Marketing Status
Marketed Since 2023-04-12
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": "c4b53c3e-e0c7-4368-beda-8c27a32ad5c9", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349479"], "spl_set_id": ["8791997d-3b86-45af-988f-808e259da506"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9696-1)", "package_ndc": "71335-9696-1", "marketing_start_date": "20230412"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "71335-9696_c4b53c3e-e0c7-4368-beda-8c27a32ad5c9", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-9696", "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": "10 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}