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
- 71205-736_a72a1311-aa68-4567-ac58-97081f675d73
- Product NDC
- 71205-736
- Form
- TABLET
- Composition / generic term
- Tadalafil
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190326
- Source listing expiry
- 20261231
Source-listed ingredients
- TADALAFIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (71205-736-10) · 71205-736-10
- 14 TABLET in 1 BOTTLE (71205-736-14) · 71205-736-14
- 15 TABLET in 1 BOTTLE (71205-736-15) · 71205-736-15
- 20 TABLET in 1 BOTTLE (71205-736-20) · 71205-736-20
- 30 TABLET in 1 BOTTLE (71205-736-30) · 71205-736-30
- 60 TABLET in 1 BOTTLE (71205-736-60) · 71205-736-60
- 90 TABLET in 1 BOTTLE (71205-736-90) · 71205-736-90
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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