Package 50268-717-15

Brand: sildenafil

Generic: sildenafil
NDC Package

Package 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
Marketed Since 2015-05-29
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"}