United States · FDA National Drug Code directory

Dabigatran Etexilate

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
62332-634_7057c0da-54c3-4021-a4de-e948a7684dc2
Product NDC
62332-634
Form
CAPSULE
Composition / generic term
Dabigatran Etexilate
Labeler
Alembic Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20240614
Source listing expiry
20261231

Source-listed ingredients

  • DABIGATRAN ETEXILATE MESYLATE — 75 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 BLISTER PACK in 1 CARTON (62332-634-06) / 6 CAPSULE in 1 BLISTER PACK · 62332-634-06
  • 60 CAPSULE in 1 BOTTLE (62332-634-60) · 62332-634-60

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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Dabigatran Etexilate — United States | Molindra Medicines