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
- 63187-813_46ab16a5-1f10-4772-97c6-272c4d28164e
- Product NDC
- 63187-813
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140103
- Source listing expiry
- 20261231
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 (63187-813-10) · 63187-813-10
- 30 TABLET, FILM COATED in 1 BOTTLE (63187-813-30) · 63187-813-30
- 50 TABLET, FILM COATED in 1 BOTTLE (63187-813-50) · 63187-813-50
- 60 TABLET, FILM COATED in 1 BOTTLE (63187-813-60) · 63187-813-60
- 90 TABLET, FILM COATED in 1 BOTTLE (63187-813-90) · 63187-813-90
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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