sildenafil citrate

Generic: sildenafil citrate

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil citrate
Generic Name sildenafil citrate
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-795
Product ID 71205-795_6fd94b93-d76c-43d0-a1cc-85fef542960e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209302
Listing Expiration 2026-12-31
Marketing Start 2020-09-04

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205795
Hyphenated Format 71205-795

Supplemental Identifiers

RxCUI
312950
UPC
0371205795306 0371205795115
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 citrate (source: ndc)
Application Number ANDA209302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (71205-795-10)
  • 1000 TABLET in 1 BOTTLE (71205-795-11)
  • 20 TABLET in 1 BOTTLE (71205-795-20)
  • 30 TABLET in 1 BOTTLE (71205-795-30)
  • 60 TABLET in 1 BOTTLE (71205-795-60)
  • 90 TABLET in 1 BOTTLE (71205-795-90)
source: ndc

Packages (6)

71205-795-10 10 TABLET in 1 BOTTLE (71205-795-10) 71205-795-11 1000 TABLET in 1 BOTTLE (71205-795-11) 71205-795-20 20 TABLET in 1 BOTTLE (71205-795-20) 71205-795-30 30 TABLET in 1 BOTTLE (71205-795-30) 71205-795-60 60 TABLET in 1 BOTTLE (71205-795-60) 71205-795-90 90 TABLET in 1 BOTTLE (71205-795-90)

Ingredients (1)

sildenafil citrate (50 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": "6fd94b93-d76c-43d0-a1cc-85fef542960e", "openfda": {"upc": ["0371205795306", "0371205795115"], "unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["8780c159-8b61-402b-afbe-64f5c85d3886"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-795-10)", "package_ndc": "71205-795-10", "marketing_start_date": "20230420"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71205-795-11)", "package_ndc": "71205-795-11", "marketing_start_date": "20251030"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-795-20)", "package_ndc": "71205-795-20", "marketing_start_date": "20230420"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-795-30)", "package_ndc": "71205-795-30", "marketing_start_date": "20230420"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-795-60)", "package_ndc": "71205-795-60", "marketing_start_date": "20230420"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-795-90)", "package_ndc": "71205-795-90", "marketing_start_date": "20230420"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "71205-795_6fd94b93-d76c-43d0-a1cc-85fef542960e", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71205-795", "generic_name": "SILDENAFIL CITRATE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL CITRATE", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA209302", "marketing_category": "ANDA", "marketing_start_date": "20200904", "listing_expiration_date": "20261231"}