United States · FDA National Drug Code directory
Vardenafil Hydrochloride
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
- 33342-154_b02d220c-5dd4-4557-880a-7d4c0d8927b9
- Product NDC
- 33342-154
- Form
- TABLET
- Composition / generic term
- Vardenafil Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191024
- Source listing expiry
- 20261231
Source-listed ingredients
- VARDENAFIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (33342-154-07) · 33342-154-07
- 100 TABLET in 1 BOTTLE (33342-154-11) · 33342-154-11
- 5 BLISTER PACK in 1 CARTON (33342-154-31) / 10 TABLET in 1 BLISTER PACK · 33342-154-31
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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