Package 71335-9689-1

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-9689-1
Digits Only 7133596891
Product NDC 71335-9689
Product ID 71335-9689_834cdc21-877d-4687-b9e8-4d418702f261
Description

30 TABLET in 1 BOTTLE (71335-9689-1)

Marketing

Marketing Status
Marketed Since 2023-04-06
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": "834cdc21-877d-4687-b9e8-4d418702f261", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349480"], "spl_set_id": ["666a622b-2464-4c55-8c90-0f1cc85bc1e9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9689-1)", "package_ndc": "71335-9689-1", "marketing_start_date": "20230406"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "71335-9689_834cdc21-877d-4687-b9e8-4d418702f261", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-9689", "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"}