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Duloxetine

NDC 71335-2625 · Bryant Ranch Prepack

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
RouteORAL
Active ingredient(s)DULOXETINE HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
Marketing categoryANDA

Packages

71335-2625-1 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2625-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-0392 — DULOXETINE HYDROCHLORIDE, 71335-0402 — Duloxetine, 71335-0509 — DULOXETINE HYDROCHLORIDE, 71335-1445 — Duloxetine, 71335-1672 — Duloxetine, 71335-1964 — Duloxetine, 71335-2017 — Duloxetine, 71335-2537 — Duloxetine, 71335-2567 — Duloxetine, 71335-2624 — Duloxetine, 71335-3062 — Duloxetine, 71335-3163 — Duloxetine, 71610-218 — DULOXETINE HYDROCHLORIDE, 71610-401 — Duloxetine Hydrochloride, 71610-402 — Duloxetine Hydrochloride, 71610-403 — Duloxetine, 71610-736 — DULOXETINE HYDROCHLORIDE, 71610-739 — DULOXETINE HYDROCHLORIDE, 71610-743 — DULOXETINE HYDROCHLORIDE, 71610-954 — 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.