United States · FDA National Drug Code directory
VARDENAFIL
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
- 71610-477_9d2796f2-b596-4588-96c8-f99407d3e671
- Product NDC
- 71610-477
- Form
- TABLET, FILM COATED
- Composition / generic term
- VARDENAFIL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181101
- Source listing expiry
- 20261231
Source-listed ingredients
- VARDENAFIL HYDROCHLORIDE TRIHYDRATE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TABLET, FILM COATED in 1 BOTTLE (71610-477-02) · 71610-477-02
- 4 TABLET, FILM COATED in 1 BOTTLE (71610-477-04) · 71610-477-04
- 6 TABLET, FILM COATED in 1 BOTTLE (71610-477-06) · 71610-477-06
- 12 TABLET, FILM COATED in 1 BOTTLE (71610-477-12) · 71610-477-12
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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