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
- 71335-1649_841b6c33-e16d-4bbb-80df-3c35c73287d3
- Product NDC
- 71335-1649
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141126
- Source listing expiry
- 20261231
Source-listed ingredients
- SILDENAFIL CITRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET, FILM COATED in 1 BOTTLE (71335-1649-0) · 71335-1649-0
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1649-1) · 71335-1649-1
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1649-2) · 71335-1649-2
- 7 TABLET, FILM COATED in 1 BOTTLE (71335-1649-3) · 71335-1649-3
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1649-4) · 71335-1649-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1649-5) · 71335-1649-5
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1649-6) · 71335-1649-6
- 270 TABLET, FILM COATED in 1 BOTTLE (71335-1649-7) · 71335-1649-7
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1649-8) · 71335-1649-8
- 12 TABLET, FILM COATED in 1 BOTTLE (71335-1649-9) · 71335-1649-9
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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