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
68071-3586_13a1084b-7b8e-7866-e063-6394a90a3bba
Product NDC
68071-3586
Form
TABLET, FILM COATED
Composition / generic term
tadalafil
Labeler
NuCare Pharmaceuticals,Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190326
Source listing expiry
20261231

Source-listed ingredients

  • TADALAFIL — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3586-9) · 68071-3586-9

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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