Package 50268-717-15
Brand: sildenafil
Generic: sildenafilPackage Facts
Identity
Package NDC
50268-717-15
Digits Only
5026871715
Product NDC
50268-717
Description
50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-717-15) / 1 TABLET in 1 BLISTER PACK (50268-717-11)
Marketing
Marketing Status
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": "436cc2bc-6fb4-227a-e063-6294a90ae221", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["e08de794-9b7e-aae6-9c89-a0c0d090cc76"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-717-15) / 1 TABLET in 1 BLISTER PACK (50268-717-11)", "package_ndc": "50268-717-15", "marketing_start_date": "20150529"}], "brand_name": "Sildenafil", "product_id": "50268-717_436cc2bc-6fb4-227a-e063-6294a90ae221", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "50268-717", "generic_name": "Sildenafil", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA202025", "marketing_category": "ANDA", "marketing_start_date": "20150529", "listing_expiration_date": "20261231"}