duloxetine

NDC 70247-014 · Qingdao BAHEAL Pharmaceutical Co., Ltd.

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

70247-014-03 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-03)

70247-014-06 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-06)

70247-014-50 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-50)

FDA lists these products with the same active ingredient.

68788-4128 — Duloxetine, 68788-7672 — Duloxetine, 68788-7897 — DULOXETINE HYDROCHLORIDE, 68788-7935 — Duloxetine, 68788-8362 — DULOXETINE HYDROCHLORIDE, 68788-8608 — Duloxetine, 68788-8623 — Duloxetine, 68788-8782 — Duloxetine, 70247-012 — Duloxetine, 70247-013 — Duloxetine, 70518-0122 — DULOXETINE HYDROCHLORIDE, 70518-1011 — Duloxetine, 70518-1054 — Duloxetine, 70518-1139 — Duloxetine, 70518-1244 — Duloxetine, 70518-1765 — Duloxetine, 70518-2630 — Duloxetine, 70518-3287 — Duloxetine, 70518-4440 — Duloxetine, 70954-860 — Duloxetine, +188 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.