United States · FDA National Drug Code directory
tadalafil
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
- 68788-4083_fee8c2be-ccfa-4c66-abed-5e232ec762ae
- Product NDC
- 68788-4083
- Form
- TABLET, FILM COATED
- Composition / generic term
- tadalafil
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260227
- Source listing expiry
- 20271231
Source-listed ingredients
- TADALAFIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-1) · 68788-4083-1
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-3) · 68788-4083-3
- 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4083-7) · 68788-4083-7
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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