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
Routes
ORAL
Active Ingredients

sildenafil citrate 100 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-473
Product ID 71205-473_1d2a3b34-3e71-4a4b-81ed-4ff35976abc0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207178
Listing Expiration 2026-12-31
Marketing Start 2020-07-10

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205473
Hyphenated Format 71205-473

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 ANDA207178 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (71205-473-10)
  • 20 TABLET in 1 BOTTLE (71205-473-20)
  • 30 TABLET in 1 BOTTLE (71205-473-30)
  • 60 TABLET in 1 BOTTLE (71205-473-60)
  • 90 TABLET in 1 BOTTLE (71205-473-90)
source: ndc

Packages (5)

Ingredients (1)

sildenafil citrate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d2a3b34-3e71-4a4b-81ed-4ff35976abc0", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["7086e222-0f2b-4c02-84c0-4f8635c90993"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (71205-473-10)", "package_ndc": "71205-473-10", "marketing_start_date": "20200824"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71205-473-20)", "package_ndc": "71205-473-20", "marketing_start_date": "20210323"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-473-30)", "package_ndc": "71205-473-30", "marketing_start_date": "20200824"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-473-60)", "package_ndc": "71205-473-60", "marketing_start_date": "20200824"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-473-90)", "package_ndc": "71205-473-90", "marketing_start_date": "20200824"}], "brand_name": "SILDENAFIL", "product_id": "71205-473_1d2a3b34-3e71-4a4b-81ed-4ff35976abc0", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71205-473", "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": "ANDA207178", "marketing_category": "ANDA", "marketing_start_date": "20200710", "listing_expiration_date": "20261231"}