sildenafil

Generic: sildenafil

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sildenafil
Generic Name sildenafil
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sildenafil citrate 50 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1028
Product ID 71335-1028_e6ae2071-5888-4010-9a90-b4297b78bb9e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202659
Listing Expiration 2026-12-31
Marketing Start 2018-06-11

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351028
Hyphenated Format 71335-1028

Supplemental Identifiers

RxCUI
312950
UNII
BW9B0ZE037

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 ANDA202659 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1028-1)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-1028-2)
  • 15 TABLET, FILM COATED in 1 BOTTLE (71335-1028-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1028-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1028-5)
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-1028-6)
source: ndc

Packages (6)

71335-1028-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1028-1) 71335-1028-2 10 TABLET, FILM COATED in 1 BOTTLE (71335-1028-2) 71335-1028-3 15 TABLET, FILM COATED in 1 BOTTLE (71335-1028-3) 71335-1028-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1028-4) 71335-1028-5 60 TABLET, FILM COATED in 1 BOTTLE (71335-1028-5) 71335-1028-6 20 TABLET, FILM COATED in 1 BOTTLE (71335-1028-6)

Ingredients (1)

sildenafil citrate (50 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": "e6ae2071-5888-4010-9a90-b4297b78bb9e", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950"], "spl_set_id": ["e22902bd-e5a8-4df6-ae77-8a0a1484cc50"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1028-1)", "package_ndc": "71335-1028-1", "marketing_start_date": "20190712"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-1028-2)", "package_ndc": "71335-1028-2", "marketing_start_date": "20181213"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71335-1028-3)", "package_ndc": "71335-1028-3", "marketing_start_date": "20190711"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1028-4)", "package_ndc": "71335-1028-4", "marketing_start_date": "20210209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1028-5)", "package_ndc": "71335-1028-5", "marketing_start_date": "20191121"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71335-1028-6)", "package_ndc": "71335-1028-6", "marketing_start_date": "20210907"}], "brand_name": "Sildenafil", "product_id": "71335-1028_e6ae2071-5888-4010-9a90-b4297b78bb9e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "71335-1028", "generic_name": "Sildenafil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "50 mg/1"}], "application_number": "ANDA202659", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}