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Duloxetine

NDC 80425-0441 · Advanced Rx of Tennessee, 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

80425-0441-1 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-1)

80425-0441-2 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-2)

80425-0441-3 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0441-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

76420-633 — Duloxetine, 76420-634 — Duloxetine, 76420-636 — Duloxetine, 80425-0012 — Duloxetine HCL, 80425-0014 — Duloxetine HCL, 80425-0086 — Duloxetine HCL, 80425-0119 — Duloxetine, 80425-0146 — Duloxetine HCL, 80425-0311 — Duloxetine, 80425-0389 — Duloxetine, 82009-029 — DULOXETINE HYDROCHLORIDE, 82009-030 — DULOXETINE HYDROCHLORIDE, 82009-031 — DULOXETINE HYDROCHLORIDE, 82009-032 — DULOXETINE HYDROCHLORIDE, 82009-170 — Duloxetine, 82009-171 — Duloxetine, 82009-172 — Duloxetine, 82009-173 — Duloxetine, 82804-024 — DULOXETINE HYDROCHLORIDE, 85534-0016 — 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.