United States · FDA National Drug Code directory

TIADYLT ER

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
71335-9719_377c5eca-9482-002a-e063-6294a90a9454
Product NDC
71335-9719
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
diltiazem hydrochloride
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20171108
Source listing expiry
20261231

Source-listed ingredients

  • DILTIAZEM HYDROCHLORIDE — 120 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9719-1) · 71335-9719-1
  • 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9719-2) · 71335-9719-2
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-9719-3) · 71335-9719-3

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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