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
71335-3049_adbe8233-4bc1-41ee-8ef7-870ae3e369c4
Product NDC
71335-3049
Form
TABLET, FILM COATED
Composition / generic term
SILDENAFIL
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20180611
Source listing expiry
20271231

Source-listed ingredients

  • SILDENAFIL CITRATE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET, FILM COATED in 1 BOTTLE (71335-3049-0) · 71335-3049-0
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-3049-1) · 71335-3049-1
  • 5 TABLET, FILM COATED in 1 BOTTLE (71335-3049-2) · 71335-3049-2
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-3049-3) · 71335-3049-3
  • 2 TABLET, FILM COATED in 1 BOTTLE (71335-3049-4) · 71335-3049-4
  • 6 TABLET, FILM COATED in 1 BOTTLE (71335-3049-5) · 71335-3049-5
  • 20 TABLET, FILM COATED in 1 BOTTLE (71335-3049-6) · 71335-3049-6
  • 4 TABLET, FILM COATED in 1 BOTTLE (71335-3049-7) · 71335-3049-7
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-3049-8) · 71335-3049-8
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-3049-9) · 71335-3049-9

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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