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
- 82804-024_f5e7503a-b28f-4cd0-a4ee-47bdca88d54b
- Product NDC
- 82804-024
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- DULOXETINE HYDROCHLORIDE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180521
- Source listing expiry
- 20261231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30) · 82804-024-30
- 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60) · 82804-024-60
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90) · 82804-024-90
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.
Browse United States records →