sildenafil citrate

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
TruPharma LLC

Identifiers & Regulatory

Product NDC 52817-295
Product ID 52817-295_a8abd38f-2334-34e3-e053-2a95a90acb7d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204883
Listing Expiration 2026-12-31
Marketing Start 2016-08-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52817295
Hyphenated Format 52817-295

Supplemental Identifiers

RxCUI
577033
UPC
0352817295002 0352817295903
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 citrate (source: ndc)
Generic Name sildenafil (source: ndc)
Application Number ANDA204883 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)
  • 90 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)
source: ndc

Packages (2)

52817-295-00 1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00) 52817-295-90 90 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)

Ingredients (1)

sildenafil citrate (20 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": "a8abd38f-2334-34e3-e053-2a95a90acb7d", "openfda": {"upc": ["0352817295002", "0352817295903"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["c8864c64-22ad-402b-a1e8-cfb53fa02e80"], "manufacturer_name": ["TruPharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (52817-295-00)", "package_ndc": "52817-295-00", "marketing_start_date": "20160801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (52817-295-90)", "package_ndc": "52817-295-90", "marketing_start_date": "20160801"}], "brand_name": "Sildenafil Citrate", "product_id": "52817-295_a8abd38f-2334-34e3-e053-2a95a90acb7d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "52817-295", "generic_name": "Sildenafil", "labeler_name": "TruPharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil Citrate", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA204883", "marketing_category": "ANDA", "marketing_start_date": "20160801", "listing_expiration_date": "20261231"}