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
- 71335-1587_3b6bc9dc-1670-4e55-8cf6-7221589070ef
- Product NDC
- 71335-1587
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tadalafil
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190327
- Source listing expiry
- 20271231
Source-listed ingredients
- TADALAFIL — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1587-1) · 71335-1587-1
- 10 TABLET, FILM COATED in 1 BOTTLE (71335-1587-2) · 71335-1587-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1587-3) · 71335-1587-3
- 5 TABLET, FILM COATED in 1 BOTTLE (71335-1587-4) · 71335-1587-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1587-5) · 71335-1587-5
- 20 TABLET, FILM COATED in 1 BOTTLE (71335-1587-6) · 71335-1587-6
- 15 TABLET, FILM COATED in 1 BOTTLE (71335-1587-7) · 71335-1587-7
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1587-8) · 71335-1587-8
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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