United States · FDA National Drug Code directory

Bosentan

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
68180-340_063d2028-f666-4304-8cd3-21d882d8c97f
Product NDC
68180-340
Form
TABLET, FOR SUSPENSION
Composition / generic term
Bosentan
Labeler
Lupin Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250818
Source listing expiry
20261231

Source-listed ingredients

  • BOSENTAN — 32 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 4 BLISTER PACK in 1 CARTON (68180-340-13) / 14 TABLET, FOR SUSPENSION in 1 BLISTER PACK · 68180-340-13

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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Bosentan — United States | Molindra Medicines