Package 51655-172-20

Brand: sildenafil

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 51655-172-20
Digits Only 5165517220
Product NDC 51655-172
Description

20 TABLET in 1 BOTTLE, PLASTIC (51655-172-20)

Marketing

Marketing Status
Marketed Since 2023-04-19
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": "48c3f84b-f73b-78b6-e063-6394a90abf6a", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["fa14cb6b-0fa8-0ba0-e053-6294a90afae3"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (51655-172-20)", "package_ndc": "51655-172-20", "marketing_start_date": "20230419"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-172-52)", "package_ndc": "51655-172-52", "marketing_start_date": "20230419"}], "brand_name": "Sildenafil", "product_id": "51655-172_48c3f84b-f73b-78b6-e063-6394a90abf6a", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "51655-172", "generic_name": "Sildenafil", "labeler_name": "Northwind Health Company, LLC", "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": "20230419", "listing_expiration_date": "20271231"}