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
- 71205-268_cfe4f78a-2bff-4f77-a582-f9027a8eb62e
- Product NDC
- 71205-268
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tadalafil
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190327
- Source listing expiry
- 20261231
Source-listed ingredients
- TADALAFIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET, FILM COATED in 1 BOTTLE (71205-268-10) · 71205-268-10
- 30 TABLET, FILM COATED in 1 BOTTLE (71205-268-30) · 71205-268-30
- 60 TABLET, FILM COATED in 1 BOTTLE (71205-268-60) · 71205-268-60
- 90 TABLET, FILM COATED in 1 BOTTLE (71205-268-90) · 71205-268-90
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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