United States · FDA National Drug Code directory

Amiodarone Hydrochloride

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
75907-005_e0bc8f4a-dc9b-7804-4479-ebe732449569
Product NDC
75907-005
Form
TABLET
Composition / generic term
Amiodarone Hydrochloride
Labeler
Dr. Reddy's Labratories Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240315 / 20270630

Source-listed ingredients

  • AMIODARONE HYDROCHLORIDE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE, PLASTIC (75907-005-30) · 75907-005-30

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.

Browse United States records →