Package 50090-5415-0

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 50090-5415-0
Digits Only 5009054150
Product NDC 50090-5415
Description

10 TABLET, FILM COATED in 1 BOTTLE (50090-5415-0)

Marketing

Marketing Status
Marketed Since 2020-12-22
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": "13483d93-57aa-42a6-86ea-ad308c07321a", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["997197bf-7706-4e12-97df-b0a9ea6d3a10"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-5415-0)", "package_ndc": "50090-5415-0", "marketing_start_date": "20201222"}], "brand_name": "Sildenafil", "product_id": "50090-5415_13483d93-57aa-42a6-86ea-ad308c07321a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50090-5415", "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": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}