United States · FDA National Drug Code directory
Duloxetine
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
- 25000-609_c8aa863f-eb1f-4b66-9ec6-2af2c7958248
- Product NDC
- 25000-609
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Duloxetine Hydrochloride
- Labeler
- MARKSANS PHARMA LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220527
- 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 (25000-609-03) · 25000-609-03
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-609-07) · 25000-609-07
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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