Package 82804-251-11

Brand: sildenafil citrate

Generic: sildenafil citrate
NDC Package

Package Facts

Identity

Package NDC 82804-251-11
Digits Only 8280425111
Product NDC 82804-251
Product ID 82804-251_1add0cab-8873-4cd1-ab53-e05c4ac458b1
Description

1000 TABLET in 1 BOTTLE (82804-251-11)

Marketing

Marketing Status
Marketed Since 2025-10-30
Brand sildenafil citrate
Generic sildenafil citrate
Sample Package No

Linked Drug Pages (1)

SILDENAFIL CITRATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1add0cab-8873-4cd1-ab53-e05c4ac458b1", "openfda": {"upc": ["0382804251117"], "unii": ["BW9B0ZE037"], "rxcui": ["314228"], "spl_set_id": ["1add0cab-8873-4cd1-ab53-e05c4ac458b1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-251-11)", "package_ndc": "82804-251-11", "marketing_start_date": "20251030"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "82804-251_1add0cab-8873-4cd1-ab53-e05c4ac458b1", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82804-251", "generic_name": "SILDENAFIL CITRATE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL CITRATE", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "25 mg/1"}], "application_number": "ANDA209302", "marketing_category": "ANDA", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}