sildenafil
Generic: sildenafil
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
sildenafil
Generic Name
sildenafil
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
sildenafil citrate 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82804-185
Product ID
82804-185_3c68969c-9034-4913-8ba1-5b0a43234ead
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210394
Listing Expiration
2026-12-31
Marketing Start
2018-05-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82804185
Hyphenated Format
82804-185
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA210394 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (82804-185-30)
- 90 TABLET in 1 BOTTLE (82804-185-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c68969c-9034-4913-8ba1-5b0a43234ead", "openfda": {"upc": ["0382804185900"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["7dd302cd-b84d-4d7d-bd1e-2916febbaea5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-185-30)", "package_ndc": "82804-185-30", "marketing_start_date": "20250806"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-185-90)", "package_ndc": "82804-185-90", "marketing_start_date": "20250206"}], "brand_name": "Sildenafil", "product_id": "82804-185_3c68969c-9034-4913-8ba1-5b0a43234ead", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "82804-185", "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": "ANDA210394", "marketing_category": "ANDA", "marketing_start_date": "20180504", "listing_expiration_date": "20261231"}