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DULOXETINE HYDROCHLORIDE

NDC 46708-278 · Alembic Pharmaceuticals Limited

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

46708-278-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-30)

46708-278-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-60)

46708-278-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-90)

46708-278-91 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 43547-381 — 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, 47335-619 — Duloxetine, 49252-007 — 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.