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Duloxetine

NDC 0615-8494 · NCS HealthCare of KY, LLC dba Vangard Labs

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

0615-8494-39 — 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8494-39)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0002-3235 — Duloxetine hydrochloride, 0002-3240 — Duloxetine hydrochloride, 0002-3270 — Duloxetine hydrochloride, 0228-2890 — Duloxetine, 0228-2891 — Duloxetine, 0228-2892 — 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, 27241-099 — Duloxetine, 27241-164 — Duloxetine, 31722-168 — Duloxetine, 31722-169 — Duloxetine, 31722-170 — Duloxetine, 33342-160 — Duloxetine Hydrochloride, 33342-161 — Duloxetine Hydrochloride, +188 more

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