sildenafil

Generic: sildenafil

Labeler: trupharma llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler trupharma llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
TruPharma LLC

Identifiers & Regulatory

Product NDC 52817-341
Product ID 52817-341_294da798-e782-4269-e063-6394a90a4b35
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204882
Listing Expiration 2026-12-31
Marketing Start 2018-07-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817341
Hyphenated Format 52817-341

Supplemental Identifiers

RxCUI
312950 314228 314229
UPC
0352817342300 0352817340306 0352817341303
UNII
BW9B0ZE037

Packaging Origin

Original Packager
true

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 ANDA204882 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (52817-341-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (52817-341-30)
source: ndc

Packages (2)

Ingredients (1)

sildenafil citrate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "294da798-e782-4269-e063-6394a90a4b35", "openfda": {"upc": ["0352817342300", "0352817340306", "0352817341303"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["53078688-ad66-4bb2-808c-b76acedd00e3"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (52817-341-10)", "package_ndc": "52817-341-10", "marketing_start_date": "20180701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (52817-341-30)", "package_ndc": "52817-341-30", "marketing_start_date": "20180701"}], "brand_name": "SILDENAFIL", "product_id": "52817-341_294da798-e782-4269-e063-6394a90a4b35", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "52817-341", "generic_name": "sildenafil", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SILDENAFIL", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA204882", "marketing_category": "ANDA", "marketing_start_date": "20180701", "listing_expiration_date": "20261231"}