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Duloxetine

NDC 63629-1991 · Bryant Ranch Prepack

Generic nameDULOXETINE HYDROCHLORIDE
Dosage formCAPSULE, DELAYED RELEASE PELLETS
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

63629-1991-1 — 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-1991-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60760-759 — Duloxetine, 62332-278 — Duloxetine, 62332-279 — Duloxetine, 62332-280 — Duloxetine, 63187-612 — Duloxetine Hydrochloride, 63187-666 — Duloxetine Hydrochloride, 63187-702 — DULOXETINE HYDROCHLORIDE, 63187-720 — DULOXETINE HYDROCHLORIDE, 63187-735 — DULOXETINE HYDROCHLORIDE, 63629-1990 — DULOXETINE HYDROCHLORIDE, 63629-1992 — DULOXETINE HYDROCHLORIDE, 63629-2063 — DULOXETINE HYDROCHLORIDE, 63629-8748 — Duloxetine, 63629-9187 — DULOXETINE HYDROCHLORIDE, 65841-799 — Duloxetine, 65841-800 — Duloxetine, 65841-801 — Duloxetine, 67046-1451 — Duloxetine, 67046-1585 — Duloxetine, 67046-1598 — 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.