United States · FDA National Drug Code directory

Orenitram

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
66302-363_bd66c62e-4aee-4fd0-bc7d-f78994dd9e29
Product NDC
66302-363
Form
KIT
Composition / generic term
treprostinil
Labeler
United Therapeutics Corporation
Marketing category
NDA
Marketing start / end (source format)
20230214
Source listing expiry
20261231

Source-listed ingredients

Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 KIT in 1 PACKAGE (66302-363-84) * 42 TABLET, EXTENDED RELEASE in 1 BLISTER PACK * 84 TABLET, EXTENDED RELEASE in 1 BLISTER PACK * 126 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 66302-363-84

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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