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 20 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-789
Product ID 63187-789_ab4d1c94-4535-4233-8521-6ec8059b7a05
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202025
Listing Expiration 2026-12-31
Marketing Start 2012-11-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187789
Hyphenated Format 63187-789

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
  • 10 TABLET in 1 BOTTLE (63187-789-10)
  • 20 TABLET in 1 BOTTLE (63187-789-20)
  • 30 TABLET in 1 BOTTLE (63187-789-30)
  • 50 TABLET in 1 BOTTLE (63187-789-50)
  • 60 TABLET in 1 BOTTLE (63187-789-60)
  • 90 TABLET in 1 BOTTLE (63187-789-90)
source: ndc

Packages (6)

63187-789-10 10 TABLET in 1 BOTTLE (63187-789-10) 63187-789-20 20 TABLET in 1 BOTTLE (63187-789-20) 63187-789-30 30 TABLET in 1 BOTTLE (63187-789-30) 63187-789-50 50 TABLET in 1 BOTTLE (63187-789-50) 63187-789-60 60 TABLET in 1 BOTTLE (63187-789-60) 63187-789-90 90 TABLET in 1 BOTTLE (63187-789-90)

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": "ab4d1c94-4535-4233-8521-6ec8059b7a05", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["38a5592a-c14a-40af-a19a-588cb11090ed"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (63187-789-10)", "package_ndc": "63187-789-10", "marketing_start_date": "20180101"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-789-20)", "package_ndc": "63187-789-20", "marketing_start_date": "20181101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-789-30)", "package_ndc": "63187-789-30", "marketing_start_date": "20161201"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (63187-789-50)", "package_ndc": "63187-789-50", "marketing_start_date": "20161201"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-789-60)", "package_ndc": "63187-789-60", "marketing_start_date": "20161201"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-789-90)", "package_ndc": "63187-789-90", "marketing_start_date": "20161201"}], "brand_name": "Sildenafil", "product_id": "63187-789_ab4d1c94-4535-4233-8521-6ec8059b7a05", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "63187-789", "generic_name": "Sildenafil", "labeler_name": "Proficient Rx LP", "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": "20121108", "listing_expiration_date": "20261231"}