sildenafil citrate

Generic: sildenafil

Labeler: northwind health company, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil citrate
Generic Name sildenafil
Labeler northwind health company, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-793
Product ID 51655-793_4973b481-9749-d08d-e063-6294a90a4ee7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204883
Listing Expiration 2027-12-31
Marketing Start 2022-01-20

Pharmacologic Class

Classes
phosphodiesterase 5 inhibitor [epc] phosphodiesterase 5 inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655793
Hyphenated Format 51655-793

Supplemental Identifiers

RxCUI
577033
UNII
BW9B0ZE037

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sildenafil citrate (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA204883 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-52)
source: ndc

Packages (2)

51655-793-20 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-20) 51655-793-52 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-793-52)

Ingredients (1)

sildenafil citrate (20 mg/1)

Linked Drug Pages (1)

Sildenafil Citrate ndc-match (0.9)

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"}