United States · FDA National Drug Code directory

Sildenafil Citrate

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
68788-8301_73d72970-dfdf-463a-af2e-e8334bb3bf5a
Product NDC
68788-8301
Form
TABLET, FILM COATED
Composition / generic term
Sildenafil
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20221130
Source listing expiry
20271231

Source-listed ingredients

  • SILDENAFIL CITRATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 TABLET, FILM COATED in 1 BOTTLE (68788-8301-1) · 68788-8301-1
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8301-3) · 68788-8301-3
  • 7 TABLET, FILM COATED in 1 BOTTLE (68788-8301-7) · 68788-8301-7

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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