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
- 33342-042_e89d523d-8d42-4bbf-be3d-2b15e7c15f4f
- Product NDC
- 33342-042
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sildenafil
- Labeler
- Macleods Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230419
- Source listing expiry
- 20261231
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 (33342-042-07) · 33342-042-07
- 100 TABLET, FILM COATED in 1 BOTTLE (33342-042-11) · 33342-042-11
- 1000 TABLET, FILM COATED in 1 BOTTLE (33342-042-44) · 33342-042-44
- 1 BLISTER PACK in 1 CARTON (33342-042-98) / 60 TABLET, FILM COATED in 1 BLISTER PACK · 33342-042-98
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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