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
- 82647-212_49fd0cc5-980e-c7d1-e063-6394a90a85c0
- Product NDC
- 82647-212
- Form
- TABLET, FILM COATED
- Composition / generic term
- sildenafil
- Labeler
- Reyoung Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220328
- Source listing expiry
- 20271231
Source-listed ingredients
- SILDENAFIL CITRATE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (82647-212-14) · 82647-212-14
- 30 TABLET, FILM COATED in 1 BOTTLE (82647-212-30) · 82647-212-30
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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