United States · FDA National Drug Code directory
Duloxetine D/R
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
- 72189-615_35ced01c-03fc-4779-e063-6394a90a9cd5
- Product NDC
- 72189-615
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Duloxetine D/R
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250217
- Source listing expiry
- 20261231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-30) · 72189-615-30
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-60) · 72189-615-60
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-615-90) · 72189-615-90
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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