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
- 71335-2017_5bbd5576-705f-420f-80e0-a72d8e43c42f
- Product NDC
- 71335-2017
- Form
- CAPSULE, DELAYED RELEASE
- Composition / generic term
- Duloxetine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170316
- 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 (71335-2017-1) · 71335-2017-1
- 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2) · 71335-2017-2
- 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3) · 71335-2017-3
- 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4) · 71335-2017-4
- 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5) · 71335-2017-5
- 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-6) · 71335-2017-6
- 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-7) · 71335-2017-7
- 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8) · 71335-2017-8
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 →