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
- 71205-231_ef7e892e-40bf-4c18-a50e-ee9e2fc9b1d7
- Product NDC
- 71205-231
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171211
- Source listing expiry
- 20271231
Source-listed ingredients
- SILDENAFIL CITRATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE (71205-231-02) · 71205-231-02
- 10 TABLET, FILM COATED in 1 BOTTLE (71205-231-10) · 71205-231-10
- 20 TABLET, FILM COATED in 1 BOTTLE (71205-231-20) · 71205-231-20
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-231-30) · 71205-231-30
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-231-60) · 71205-231-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-231-90) · 71205-231-90
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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