sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-172
Product ID 51655-172_48c3f84b-f73b-78b6-e063-6394a90abf6a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202025
Listing Expiration 2027-12-31
Marketing Start 2023-04-19

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51655172
Hyphenated Format 51655-172

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 (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA202025 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE, PLASTIC (51655-172-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (51655-172-52)
source: ndc

Packages (2)

51655-172-20 20 TABLET in 1 BOTTLE, PLASTIC (51655-172-20) 51655-172-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-172-52)

Ingredients (1)

sildenafil citrate (20 mg/1)

Linked Drug Pages (1)

Sildenafil ndc-match (0.9)

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"}