United States · FDA National Drug Code directory
Duloxetine Delayed-Release
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
- 71335-0509_f56840bd-a85a-489d-ae5a-cf6fe696f1a8
- Product NDC
- 71335-0509
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- DULOXETINE HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140611
- Source listing expiry
- 20261231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-1) · 71335-0509-1
- 28 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-2) · 71335-0509-2
- 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-3) · 71335-0509-3
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-4) · 71335-0509-4
- 180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-5) · 71335-0509-5
- 120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0509-6) · 71335-0509-6
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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