Package 50090-6804-0

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 50090-6804-0
Digits Only 5009068040
Product NDC 50090-6804
Product ID 50090-6804_fe1514c6-f229-46ee-b92d-90f2f3981cce
Description

10 TABLET, FILM COATED in 1 BOTTLE (50090-6804-0)

Marketing

Marketing Status
Marketed Since 2023-11-06
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": "fe1514c6-f229-46ee-b92d-90f2f3981cce", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["e5ad3ce5-29ee-4b55-a67a-0f28c23a3afa"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-6804-0)", "package_ndc": "50090-6804-0", "marketing_start_date": "20231106"}], "brand_name": "SILDENAFIL", "product_id": "50090-6804_fe1514c6-f229-46ee-b92d-90f2f3981cce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-6804", "generic_name": "sildenafil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA204882", "marketing_category": "ANDA", "marketing_start_date": "20210617", "listing_expiration_date": "20271231"}