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
59746-471_9a1dd479-ab39-4e0e-859b-33c7d7dbbf26
Product NDC
59746-471
Form
TABLET, FILM COATED
Composition / generic term
sildenafil
Labeler
Jubilant Cadista Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240826
Source listing expiry
20271231

Source-listed ingredients

  • SILDENAFIL CITRATE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 TABLET, FILM COATED in 1 BOTTLE (59746-471-05) · 59746-471-05
  • 1000 TABLET, FILM COATED in 1 BOTTLE (59746-471-10) · 59746-471-10
  • 90 TABLET, FILM COATED in 1 BOTTLE (59746-471-90) · 59746-471-90

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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