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
- 46708-636_4f8d4596-bc1a-48a1-8f6a-caf816a2037f
- Product NDC
- 46708-636
- Form
- CAPSULE
- Composition / generic term
- Dabigatran Etexilate
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240614
- Source listing expiry
- 20261231
Source-listed ingredients
- DABIGATRAN ETEXILATE MESYLATE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (46708-636-06) / 6 CAPSULE in 1 BLISTER PACK · 46708-636-06
- 180 CAPSULE in 1 BOTTLE (46708-636-45) · 46708-636-45
- 60 CAPSULE in 1 BOTTLE (46708-636-60) · 46708-636-60
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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