United States · FDA National Drug Code directory

Sildenafil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72241-069_a177c85e-62a3-466c-af85-a4eacb06e223
Product NDC
72241-069
Form
TABLET, FILM COATED
Composition / generic term
Sildenafil
Labeler
Modavar Pharmaceuticals LLC
Marketing category
ANDA
Marketing start / end (source format)
20240214
Source listing expiry
20261231

Source-listed ingredients

  • SILDENAFIL CITRATE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

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

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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