Package 0093-7653-56

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-7653-56
Digits Only 0093765356
Product NDC 0093-7653
Product ID 0093-7653_51f4534a-5b11-490a-9e0b-ac681150967f
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-7653-56)

Marketing

Marketing Status
Marketed Since 2019-01-03
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": "51f4534a-5b11-490a-9e0b-ac681150967f", "openfda": {"upc": ["0300937654568", "0300937653561"], "unii": ["5M8S2CU0TS"], "rxcui": ["349478", "349479", "349480", "402273"], "spl_set_id": ["e593ab58-70a4-4095-8091-16a4b6d49e4d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7653-56)", "package_ndc": "0093-7653-56", "marketing_start_date": "20190103"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "0093-7653_51f4534a-5b11-490a-9e0b-ac681150967f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0093-7653", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091347", "marketing_category": "ANDA", "marketing_start_date": "20190103", "listing_expiration_date": "20261231"}