sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-220
Product ID 71205-220_5d593e03-b6f0-41d0-b7b2-e53d2421a903
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203962
Listing Expiration 2026-12-31
Marketing Start 2018-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205220
Hyphenated Format 71205-220

Supplemental Identifiers

RxCUI
314229
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 ANDA203962 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 10 TABLET, FILM COATED in 1 BOTTLE (71205-220-10)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71205-220-20)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-220-30)
  • 50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)
source: ndc

Packages (6)

71205-220-10 10 TABLET, FILM COATED in 1 BOTTLE (71205-220-10) 71205-220-20 20 TABLET, FILM COATED in 1 BOTTLE (71205-220-20) 71205-220-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-220-30) 71205-220-50 50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50) 71205-220-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60) 71205-220-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)

Ingredients (1)

sildenafil citrate (100 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": "5d593e03-b6f0-41d0-b7b2-e53d2421a903", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["61c3866e-401d-48b3-a0d2-1e24a33ab512"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71205-220-10)", "package_ndc": "71205-220-10", "marketing_start_date": "20190201"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-220-20)", "package_ndc": "71205-220-20", "marketing_start_date": "20190201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-220-30)", "package_ndc": "71205-220-30", "marketing_start_date": "20190201"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50)", "package_ndc": "71205-220-50", "marketing_start_date": "20190201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60)", "package_ndc": "71205-220-60", "marketing_start_date": "20190201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90)", "package_ndc": "71205-220-90", "marketing_start_date": "20190201"}], "brand_name": "Sildenafil", "product_id": "71205-220_5d593e03-b6f0-41d0-b7b2-e53d2421a903", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71205-220", "generic_name": "Sildenafil", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA203962", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}