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
- 50090-6889_2bcd10f1-d5c6-4886-ac10-39e7a658448d
- Product NDC
- 50090-6889
- Form
- CAPSULE, DELAYED RELEASE PELLETS
- Composition / generic term
- DULOXETINE HYDROCHLORIDE
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140611
- Source listing expiry
- 20261231
Source-listed ingredients
- DULOXETINE HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-0) · 50090-6889-0
- 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-1) · 50090-6889-1
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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