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
27241-124_f5da6ecc-eebe-409e-9251-869a73ef4d4e
Product NDC
27241-124
Form
TABLET
Composition / generic term
Sildenafil
Labeler
Ajanta Pharma USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20180504
Source listing expiry
20261231

Source-listed ingredients

  • SILDENAFIL CITRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 BOTTLE (27241-124-03) · 27241-124-03
  • 500 TABLET in 1 BOTTLE (27241-124-05) · 27241-124-05

Source and coverage

Open FDA National Drug Code directory

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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