The short version
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Duloxetine D/R
Duloxetine D/R · DULOXETINE HYDROCHLORIDE 30 mg/1 · Capsule, Delayed Release · Oral · Direct_Rx
NDC 72189-0615-30 · 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE · ANDA · View full market →
Medicare Part D
No Medicare Part D plan in CMS's quarterly files lists this product. That usually means it is discontinued, a repackager's listing, or a product no plan has added to its formulary.
How Part D pricing works →NADAC price per unit
No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.
Supply fragility
Not scored — fragility is computed for NADAC-priced NDCs.
Where it's made
- Direct RxUnited Statesrepack
Establishments this product's FDA label declares, located via FDA registration data. How we built this →
Regulatory
- Application
- ANDA090694
- TE code
- AB
- Approval date
- Dec 11, 2013
- Patents / exclusivity
- None on file
Shortage history
No FDA shortage reports for this drug or its presentations.
Recalls (this NDC)
No enforcement reports list this package NDC.
Manufacturers of Duloxetine D/R (Capsule, Delayed Release)
| Labeler | Strength | First seen | Last seen |
|---|---|---|---|
| Direct_Rx | DULOXETINE HYDROCHLORIDE 20 mg/1 | Jul 15, 2026 | Sep 2, 2026 |
| Direct_Rx | DULOXETINE HYDROCHLORIDE 60 mg/1 | Jul 15, 2026 | Sep 2, 2026 |
| Direct_Rx | DULOXETINE HYDROCHLORIDE 30 mg/1 | Jul 15, 2026 | Aug 31, 2026 |
Roster from daily NDC Directory diffs — first/last seen dates start July 2026.
Cite this page
DrugDashboards, "Duloxetine D/R — NDC 72189-0615-30," retrieved September 3, 2026, https://drugdashboards.com/drug/72189061530.
Free to cite with attribution — see how the data is put together.