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: 29300-289_6fee8842-9e23-43d9-a4ff-4e147bf9f6a1
Product NDC: 29300-289
Form: TABLET, FILM COATED
Composition / generic term: tadalafil
Labeler: Unichem Pharmaceuticals (USA), Inc.
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

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-01) · 29300-289-01
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-05) · 29300-289-05
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-289-13) · 29300-289-13

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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