sildenafil

Generic: sildenafil

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

Drug Facts

Product Profile

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

sildenafil citrate 25 mg/1

Manufacturer
Modavar Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72241-069
Product ID 72241-069_a177c85e-62a3-466c-af85-a4eacb06e223
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA218045
Listing Expiration 2026-12-31
Marketing Start 2024-02-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72241069
Hyphenated Format 72241-069

Supplemental Identifiers

RxCUI
312950 314228 314229
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 ANDA218045 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (72241-069-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (72241-069-11)
  • 30 TABLET, FILM COATED in 1 BOTTLE (72241-069-22)
source: ndc

Packages (3)

72241-069-05 100 TABLET, FILM COATED in 1 BOTTLE (72241-069-05) 72241-069-11 1000 TABLET, FILM COATED in 1 BOTTLE (72241-069-11) 72241-069-22 30 TABLET, FILM COATED in 1 BOTTLE (72241-069-22)

Ingredients (1)

sildenafil citrate (25 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": "a177c85e-62a3-466c-af85-a4eacb06e223", "openfda": {"unii": ["BW9B0ZE037"], "rxcui": ["312950", "314228", "314229"], "spl_set_id": ["8c4f22c8-3607-4d64-8821-dd3202f8fa0a"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72241-069-05)", "package_ndc": "72241-069-05", "marketing_start_date": "20240214"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72241-069-11)", "package_ndc": "72241-069-11", "marketing_start_date": "20240214"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72241-069-22)", "package_ndc": "72241-069-22", "marketing_start_date": "20240214"}], "brand_name": "Sildenafil", "product_id": "72241-069_a177c85e-62a3-466c-af85-a4eacb06e223", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "72241-069", "generic_name": "Sildenafil", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sildenafil", "active_ingredients": [{"name": "SILDENAFIL CITRATE", "strength": "25 mg/1"}], "application_number": "ANDA218045", "marketing_category": "ANDA", "marketing_start_date": "20240214", "listing_expiration_date": "20261231"}