United States · FDA National Drug Code directory

Ursodiol

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
24658-999_8f808940-188e-4624-aee2-a84e3d7b58d7
Product NDC
24658-999
Form
CAPSULE
Composition / generic term
Ursodiol
Labeler
PuraCap Laboratories, LLC
Marketing category
ANDA
Marketing start / end (source format)
20210930
Source listing expiry
20261231

Source-listed ingredients

  • URSODIOL — 300 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 CAPSULE in 1 BOTTLE (24658-999-10) · 24658-999-10

Source and coverage

Open FDA National Drug Code directory

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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