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
- 60290-002_51b76a30-43fd-eaa4-e063-6394a90a286d
- Product NDC
- 60290-002
- Form
- TABLET, FILM COATED
- Composition / generic term
- SILDENAFIL CITRATE
- Labeler
- Umedica Laboratories USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260215
- Source listing expiry
- 20271231
Source-listed ingredients
- SILDENAFIL CITRATE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (60290-002-01) · 60290-002-01
- 100 TABLET, FILM COATED in 1 BOTTLE (60290-002-02) · 60290-002-02
- 1000 TABLET, FILM COATED in 1 BOTTLE (60290-002-03) · 60290-002-03
- 500 TABLET, FILM COATED in 1 BOTTLE (60290-002-04) · 60290-002-04
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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