Package 42291-826-30

Brand: vardenafil hydrochloride

Generic: vardenafil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42291-826-30
Digits Only 4229182630
Product NDC 42291-826
Product ID 42291-826_3b038d71-adaa-fc9a-e063-6294a90abe6a
Description

30 TABLET in 1 BOTTLE (42291-826-30)

Marketing

Marketing Status
Marketed Since 2025-07-28
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": "3b038d71-adaa-fc9a-e063-6294a90abe6a", "openfda": {"upc": ["0342291847309"], "unii": ["5M8S2CU0TS"], "rxcui": ["349478"], "spl_set_id": ["3b03952b-d404-09cd-e063-6294a90a8b2c"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42291-826-30)", "package_ndc": "42291-826-30", "marketing_start_date": "20250728"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "42291-826_3b038d71-adaa-fc9a-e063-6294a90abe6a", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "42291-826", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20250728", "listing_expiration_date": "20261231"}