Duloxetine

NDC 82009-172 · Quallent Pharmaceuticals Health LLC

Generic nameDuloxetine

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)DULOXETINE HYDROCHLORIDE

Strength40 mg/1

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

Marketing categoryANDA

Packages

82009-172-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-172-30)

FDA lists these products with the same active ingredient.

80425-0146 — Duloxetine HCL, 80425-0311 — Duloxetine, 80425-0389 — Duloxetine, 80425-0441 — Duloxetine, 82009-029 — DULOXETINE HYDROCHLORIDE, 82009-030 — DULOXETINE HYDROCHLORIDE, 82009-031 — DULOXETINE HYDROCHLORIDE, 82009-032 — DULOXETINE HYDROCHLORIDE, 82009-170 — Duloxetine, 82009-171 — Duloxetine, 82009-173 — Duloxetine, 82804-024 — DULOXETINE HYDROCHLORIDE, 85534-0016 — Duloxetine, 85534-0017 — Duloxetine, 85534-0018 — Duloxetine, 85534-0050 — Duloxetine, 85534-0051 — Duloxetine, 85534-0052 — Duloxetine, 85534-0053 — Duloxetine, 87063-702 — Duloxetine, +188 more

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