sildenafil

Generic: sildenafil

Labeler: teva pharmaceuticals usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler teva pharmaceuticals usa, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 20 mg/1

Manufacturer
Teva Pharmaceuticals USA, Inc.

Identifiers & Regulatory

Product NDC 0093-5517
Product ID 0093-5517_dc1607a4-e925-4265-b498-53c3936cddb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078380
Marketing Start 2013-05-31
Marketing End 2026-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00935517
Hyphenated Format 0093-5517

Supplemental Identifiers

RxCUI
577033
UPC
0300935517988
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 ANDA078380 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)
source: ndc

Packages (1)

0093-5517-98 90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)

Ingredients (1)

sildenafil citrate (20 mg/1)

Linked Drug Pages (1)

Sildenafil ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dc1607a4-e925-4265-b498-53c3936cddb7", "openfda": {"upc": ["0300935517988"], "unii": ["BW9B0ZE037"], "rxcui": ["577033"], "spl_set_id": ["2582414d-0ef3-403e-84e8-1d6c812e7eb1"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0093-5517-98)", "package_ndc": "0093-5517-98", "marketing_end_date": "20260331", "marketing_start_date": "20130531"}], "brand_name": "Sildenafil", "product_id": "0093-5517_dc1607a4-e925-4265-b498-53c3936cddb7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "0093-5517", "generic_name": "Sildenafil", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "ANDA078380", "marketing_category": "ANDA", "marketing_end_date": "20260331", "marketing_start_date": "20130531"}