Package 82804-243-30

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 82804-243-30
Digits Only 8280424330
Product NDC 82804-243
Description

30 TABLET, FILM COATED in 1 BOTTLE (82804-243-30)

Marketing

Marketing Status
Marketed Since 2025-09-10
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": "71140bd5-0a51-4c01-ad0d-193d08ea67dd", "openfda": {"upc": ["0382804243303"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["71140bd5-0a51-4c01-ad0d-193d08ea67dd"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82804-243-30)", "package_ndc": "82804-243-30", "marketing_start_date": "20250910"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-243-90)", "package_ndc": "82804-243-90", "marketing_start_date": "20250915"}], "brand_name": "Sildenafil", "product_id": "82804-243_71140bd5-0a51-4c01-ad0d-193d08ea67dd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82804-243", "generic_name": "Sildenafil", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA091479", "marketing_category": "ANDA", "marketing_start_date": "20121106", "listing_expiration_date": "20261231"}