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 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-251
Product ID 82804-251_1add0cab-8873-4cd1-ab53-e05c4ac458b1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209302
Listing Expiration 2026-12-31
Marketing Start 2021-06-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804251
Hyphenated Format 82804-251

Supplemental Identifiers

RxCUI
314228
UPC
0382804251117
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
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (82804-251-11)
source: ndc

Packages (1)

Ingredients (1)

sildenafil citrate (25 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1add0cab-8873-4cd1-ab53-e05c4ac458b1", "openfda": {"upc": ["0382804251117"], "unii": ["BW9B0ZE037"], "rxcui": ["314228"], "spl_set_id": ["1add0cab-8873-4cd1-ab53-e05c4ac458b1"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-251-11)", "package_ndc": "82804-251-11", "marketing_start_date": "20251030"}], "brand_name": "SILDENAFIL CITRATE", "product_id": "82804-251_1add0cab-8873-4cd1-ab53-e05c4ac458b1", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82804-251", "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": "25 mg/1"}], "application_number": "ANDA209302", "marketing_category": "ANDA", "marketing_start_date": "20210616", "listing_expiration_date": "20261231"}