Duloxetine

NDC 27241-099 · Ajanta Pharma USA 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

27241-099-03 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-03)

27241-099-40 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-40)

27241-099-90 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-90)

FDA lists these products with the same active ingredient.

0228-2891 — Duloxetine, 0228-2892 — Duloxetine, 0615-8494 — Duloxetine, 0615-8495 — Duloxetine, 0615-8496 — Duloxetine, 25000-608 — Duloxetine Hydrochloride, 25000-609 — Duloxetine Hydrochloride, 25000-610 — Duloxetine Hydrochloride, 27241-097 — Duloxetine, 27241-098 — 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, 43547-380 — 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.