Package 71335-9688-1

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-9688-1
Digits Only 7133596881
Product NDC 71335-9688
Product ID 71335-9688_5b030c96-c5e2-4cde-abda-d6eedff4169d
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-9688-1)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "5b030c96-c5e2-4cde-abda-d6eedff4169d", "openfda": {"unii": ["5M8S2CU0TS"], "rxcui": ["349480"], "spl_set_id": ["31be68b0-ac7e-42d0-9435-1f0a329b63d8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-9688-1)", "package_ndc": "71335-9688-1", "marketing_start_date": "20240403"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "71335-9688_5b030c96-c5e2-4cde-abda-d6eedff4169d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-9688", "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": "ANDA091347", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}