Skip to main content

Duloxetine

NDC 71335-1672 · Bryant Ranch Prepack

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

71335-1672-1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-1)

71335-1672-2 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-2)

71335-1672-3 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-3)

71335-1672-4 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-4)

71335-1672-5 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-5)

71335-1672-6 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-6)

71335-1672-7 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-7)

71335-1672-8 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-005 — Duloxetine, 71205-358 — Duloxetine, 71205-445 — Duloxetine, 71205-525 — Duloxetine, 71205-602 — Duloxetine, 71335-0165 — DULOXETINE HYDROCHLORIDE, 71335-0392 — DULOXETINE HYDROCHLORIDE, 71335-0402 — Duloxetine, 71335-0509 — DULOXETINE HYDROCHLORIDE, 71335-1445 — Duloxetine, 71335-1964 — Duloxetine, 71335-2017 — Duloxetine, 71335-2537 — Duloxetine, 71335-2567 — Duloxetine, 71335-2624 — Duloxetine, 71335-2625 — Duloxetine, 71335-3062 — Duloxetine, 71335-3163 — Duloxetine, 71610-218 — DULOXETINE HYDROCHLORIDE, 71610-401 — 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.