DULOXETINE HYDROCHLORIDE

NDC 62332-278 · Alembic Pharmaceuticals Inc.

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

62332-278-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-30)

62332-278-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-60)

62332-278-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-90)

62332-278-91 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-91)

FDA lists these products with the same active ingredient.

52427-791 — Duloxetine, 52427-821 — Duloxetine, 52427-913 — Duloxetine, 59651-279 — Duloxetine Hydrochloride, 59651-280 — Duloxetine Hydrochloride, 59651-282 — Duloxetine Hydrochloride, 60429-164 — DULOXETINE HYDROCHLORIDE, 60760-461 — Duloxetine, 60760-462 — Duloxetine, 60760-759 — Duloxetine, 62332-279 — Duloxetine, 62332-280 — Duloxetine, 63187-612 — Duloxetine Hydrochloride, 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, +188 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.