Package 50090-5235-0

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 50090-5235-0
Digits Only 5009052350
Product NDC 50090-5235
Product ID 50090-5235_893aeefd-b757-4d8c-8f17-711a114c0d9b
Description

10 TABLET, FILM COATED in 1 BOTTLE (50090-5235-0)

Marketing

Marketing Status
Marketed Since 2020-10-09
Brand sildenafil
Generic sildenafil
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "893aeefd-b757-4d8c-8f17-711a114c0d9b", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314228"], "spl_set_id": ["3145ceda-8c1e-4601-8a9d-5fc4978226d6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-5235-0)", "package_ndc": "50090-5235-0", "marketing_start_date": "20201009"}], "brand_name": "Sildenafil", "product_id": "50090-5235_893aeefd-b757-4d8c-8f17-711a114c0d9b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-5235", "generic_name": "Sildenafil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "25 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}