DULOXETINE

NDC 43547-380 · Solco Healthcare US, LLC

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

43547-380-03 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-380-03)

43547-380-09 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-380-09)

43547-380-11 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-380-11)

FDA lists these products with the same active ingredient.

27241-099 — Duloxetine, 27241-164 — Duloxetine, 31722-168 — Duloxetine, 31722-169 — Duloxetine, 31722-170 — Duloxetine, 33342-160 — Duloxetine Hydrochloride, 33342-161 — Duloxetine Hydrochloride, 33342-162 — Duloxetine Hydrochloride, 42708-196 — Duloxetine, 43547-379 — Duloxetine, 43547-381 — Duloxetine, 46708-278 — Duloxetine, 46708-279 — Duloxetine, 46708-280 — Duloxetine, 47335-381 — Duloxetine, 47335-382 — Duloxetine, 47335-383 — Duloxetine, 47335-616 — Duloxetine, 47335-617 — Duloxetine, 47335-618 — 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.