Skip to main content

Duloxetine

NDC 65841-799 · Zydus Lifesciences Limited

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength20 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA

Packages

65841-799-06 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06)

65841-799-14 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14)

65841-799-16 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-666 — Duloxetine Hydrochloride, 63187-702 — DULOXETINE HYDROCHLORIDE, 63187-720 — DULOXETINE HYDROCHLORIDE, 63187-735 — DULOXETINE HYDROCHLORIDE, 63629-1990 — DULOXETINE HYDROCHLORIDE, 63629-1991 — DULOXETINE HYDROCHLORIDE, 63629-1992 — DULOXETINE HYDROCHLORIDE, 63629-2063 — DULOXETINE HYDROCHLORIDE, 63629-8748 — Duloxetine, 63629-9187 — DULOXETINE HYDROCHLORIDE, 65841-800 — Duloxetine, 65841-801 — Duloxetine, 67046-1451 — Duloxetine, 67046-1585 — Duloxetine, 67046-1598 — Duloxetine, 67877-263 — Duloxetine, 67877-264 — Duloxetine, 67877-265 — Duloxetine, 68001-368 — DULOXETINE HYDROCHLORIDE, 68001-570 — Duloxetine, +188 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.