sildenafil

Generic: sildenafil

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sildenafil citrate 100 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 60219-1753
Product ID 60219-1753_8148bd41-7822-4d86-b60e-d6b01060d3a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202023
Listing Expiration 2026-12-31
Marketing Start 2018-06-28

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 602191753
Hyphenated Format 60219-1753

Supplemental Identifiers

RxCUI
312950 314228 314229
UPC
0360219175334 0360219175136 0360219175235
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 ANDA202023 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (60219-1753-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (60219-1753-3)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (60219-1753-7)
source: ndc

Packages (3)

60219-1753-1 100 TABLET, FILM COATED in 1 BOTTLE (60219-1753-1) 60219-1753-3 30 TABLET, FILM COATED in 1 BOTTLE (60219-1753-3) 60219-1753-7 1000 TABLET, FILM COATED in 1 BOTTLE (60219-1753-7)

Ingredients (1)

sildenafil citrate (100 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": "8148bd41-7822-4d86-b60e-d6b01060d3a8", "openfda": {"upc": ["0360219175334", "0360219175136", "0360219175235"], "unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["a1c3a2a2-8cf5-41c3-9c86-54290570d916"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60219-1753-1)", "package_ndc": "60219-1753-1", "marketing_start_date": "20180628"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60219-1753-3)", "package_ndc": "60219-1753-3", "marketing_start_date": "20180628"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60219-1753-7)", "package_ndc": "60219-1753-7", "marketing_start_date": "20180628"}], "brand_name": "Sildenafil", "product_id": "60219-1753_8148bd41-7822-4d86-b60e-d6b01060d3a8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "60219-1753", "generic_name": "Sildenafil", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "100 mg/1"}], "application_number": "ANDA202023", "marketing_category": "ANDA", "marketing_start_date": "20180628", "listing_expiration_date": "20261231"}