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
- 71205-220_5d593e03-b6f0-41d0-b7b2-e53d2421a903
- Product NDC
- 71205-220
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180611
- Source listing expiry
- 20261231
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 (71205-220-10) · 71205-220-10
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-220-20) · 71205-220-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-220-30) · 71205-220-30
- 50 TABLET, FILM COATED in 1 BOTTLE (71205-220-50) · 71205-220-50
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-220-60) · 71205-220-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-220-90) · 71205-220-90
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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