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
- 71335-1005_7dde9c19-f947-49da-bcd3-01430780e173
- Product NDC
- 71335-1005
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140103 / 20271031
Source-listed ingredients
- SILDENAFIL CITRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1005-1) · 71335-1005-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1005-2) · 71335-1005-2
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-1005-3) · 71335-1005-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1005-4) · 71335-1005-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1005-5) · 71335-1005-5
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1005-6) · 71335-1005-6
- 270 TABLET, FILM COATED in 1 BOTTLE (71335-1005-7) · 71335-1005-7
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1005-8) · 71335-1005-8
- 12 TABLET, FILM COATED in 1 BOTTLE (71335-1005-9) · 71335-1005-9
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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