Package 51655-793-52

Brand: sildenafil citrate

Generic: sildenafil
NDC Package

Package Facts

Identity

Package NDC 51655-793-52
Digits Only 5165579352
Product NDC 51655-793
Product ID 51655-793_4973b481-9749-d08d-e063-6294a90a4ee7
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-52)

Marketing

Marketing Status
Marketed Since 2022-01-20
Brand sildenafil citrate
Generic sildenafil
Sample Package No

Linked Drug Pages (1)

Sildenafil Citrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4973b481-9749-d08d-e063-6294a90a4ee7", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["d9ddfd2a-1961-90f9-e053-2a95a90a7f9b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20)", "package_ndc": "51655-793-20", "marketing_start_date": "20220120"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-52)", "package_ndc": "51655-793-52", "marketing_start_date": "20220120"}], "brand_name": "Sildenafil Citrate", "product_id": "51655-793_4973b481-9749-d08d-e063-6294a90a4ee7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "51655-793", "generic_name": "Sildenafil", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA204883", "marketing_category": "ANDA", "marketing_start_date": "20220120", "listing_expiration_date": "20271231"}