sildenafil

Generic: sildenafil

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

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

sildenafil citrate 20 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-0033
Product ID 59762-0033_c1cc0357-ac81-40b6-a401-dfd941495be5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021845
Marketing Start 2012-09-27
Marketing End 2026-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 597620033
Hyphenated Format 59762-0033

Supplemental Identifiers

RxCUI
577033 1307427
UPC
0359762003317
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 NDA021845 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)
source: ndc

Packages (1)

59762-0033-3 300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)

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": "c1cc0357-ac81-40b6-a401-dfd941495be5", "openfda": {"upc": ["0359762003317"], "unii": ["BW9B0ZE037"], "rxcui": ["577033", "1307427"], "spl_set_id": ["56a962e8-de00-4a97-8904-0b1bd217dd83"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET, FILM COATED in 1 BOTTLE (59762-0033-3)", "package_ndc": "59762-0033-3", "marketing_end_date": "20260731", "marketing_start_date": "20201109"}], "brand_name": "Sildenafil", "product_id": "59762-0033_c1cc0357-ac81-40b6-a401-dfd941495be5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "59762-0033", "generic_name": "sildenafil", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "20 mg/1"}], "application_number": "NDA021845", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_end_date": "20260731", "marketing_start_date": "20120927"}