Duloxetine

NDC 71205-602 · Proficient Rx LP

Generic nameDuloxetine

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)DULOXETINE HYDROCHLORIDE

Strength30 mg/1

Pharmacologic classNorepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Marketing categoryANDA

Packages

71205-602-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-30)

71205-602-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-60)

71205-602-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-602-90)

FDA lists these products with the same active ingredient.

70518-2630 — Duloxetine, 70518-3287 — Duloxetine, 70518-4440 — Duloxetine, 70954-860 — Duloxetine, 70954-861 — Duloxetine, 70954-864 — Duloxetine, 71205-005 — Duloxetine, 71205-358 — Duloxetine, 71205-445 — Duloxetine, 71205-525 — Duloxetine, 71335-0165 — DULOXETINE HYDROCHLORIDE, 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, +188 more

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