Package 71205-721-04

Brand: sildenafil citrate

Generic: sildenafil citrate
NDC Package

Package Facts

Identity

Package NDC 71205-721-04
Digits Only 7120572104
Product NDC 71205-721
Product ID 71205-721_59b623bc-fbdd-4f32-8327-0d600763f429
Description

4 TABLET in 1 BOTTLE (71205-721-04)

Marketing

Marketing Status
Marketed Since 2022-11-16
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": "59b623bc-fbdd-4f32-8327-0d600763f429", "openfda": {"upc": ["0371205721046"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["59b623bc-fbdd-4f32-8327-0d600763f429"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE (71205-721-04)", "package_ndc": "71205-721-04", "marketing_start_date": "20221116"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "71205-721_59b623bc-fbdd-4f32-8327-0d600763f429", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71205-721", "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": "50 mg/1"}], "application_number": "ANDA209302", "marketing_category": "ANDA", "marketing_start_date": "20200904", "listing_expiration_date": "20261231"}