Package 72865-105-90

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 72865-105-90
Digits Only 7286510590
Product NDC 72865-105
Description

90 TABLET, FILM COATED in 1 BOTTLE (72865-105-90)

Marketing

Marketing Status
Marketed Since 2019-07-10
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f26fd814-a6cb-4749-e053-2a95a90a26fb", "openfda": {"upc": ["0372865131305"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["22d70b8d-41bc-416d-89e9-e4c39db0af83"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72865-105-90)", "package_ndc": "72865-105-90", "marketing_start_date": "20190710"}], "brand_name": "Sildenafil", "product_id": "72865-105_f26fd814-a6cb-4749-e053-2a95a90a26fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72865-105", "generic_name": "Sildenafil", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA203623", "marketing_category": "ANDA", "marketing_start_date": "20190710", "listing_expiration_date": "20261231"}