sildenafil citrate

Generic: sildenafil citrate

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil citrate
Generic Name sildenafil citrate
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sildenafil citrate 100 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8804
Product ID 68788-8804_5846bff2-6a93-46a7-a547-04459c590814
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209302
Listing Expiration 2026-12-31
Marketing Start 2025-01-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888804
Hyphenated Format 68788-8804

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 citrate (source: ndc)
Generic Name sildenafil citrate (source: ndc)
Application Number ANDA209302 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE (68788-8804-1)
  • 30 TABLET in 1 BOTTLE (68788-8804-3)
  • 7 TABLET in 1 BOTTLE (68788-8804-7)
source: ndc

Packages (3)

68788-8804-1 10 TABLET in 1 BOTTLE (68788-8804-1) 68788-8804-3 30 TABLET in 1 BOTTLE (68788-8804-3) 68788-8804-7 7 TABLET in 1 BOTTLE (68788-8804-7)

Ingredients (1)

sildenafil citrate (100 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": "5846bff2-6a93-46a7-a547-04459c590814", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["314229"], "spl_set_id": ["5846bff2-6a93-46a7-a547-04459c590814"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (68788-8804-1)", "package_ndc": "68788-8804-1", "marketing_start_date": "20250120"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8804-3)", "package_ndc": "68788-8804-3", "marketing_start_date": "20250120"}, {"sample": false, "description": "7 TABLET in 1 BOTTLE (68788-8804-7)", "package_ndc": "68788-8804-7", "marketing_start_date": "20250120"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "68788-8804_5846bff2-6a93-46a7-a547-04459c590814", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "68788-8804", "generic_name": "SILDENAFIL CITRATE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL CITRATE", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA209302", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}