Duloxetine

NDC 42708-196 · QPharma, Inc.

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

42708-196-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-196-30)

FDA lists these products with the same active ingredient.

27241-097 — Duloxetine, 27241-098 — Duloxetine, 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, 43547-379 — Duloxetine, 43547-380 — 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, +188 more

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