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Duloxetine

NDC 51991-746 · Breckenridge Pharmaceutical, Inc.

Generic nameDULOXETINE HYDROCHLORIDE
Dosage formCAPSULE, DELAYED RELEASE PELLETS
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

51991-746-05 — 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-05)

51991-746-06 — 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-06)

51991-746-90 — 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50771-202 — DULOXETINE HYDROCHLORIDE, 50771-203 — DULOXETINE HYDROCHLORIDE, 51407-807 — Duloxetine, 51407-808 — Duloxetine, 51407-809 — Duloxetine, 51407-810 — Duloxetine, 51407-817 — DULOXETINE HYDROCHLORIDE, 51407-818 — DULOXETINE HYDROCHLORIDE, 51407-819 — DULOXETINE HYDROCHLORIDE, 51655-237 — Duloxetine, 51991-747 — DULOXETINE HYDROCHLORIDE, 51991-748 — DULOXETINE HYDROCHLORIDE, 51991-750 — DULOXETINE HYDROCHLORIDE, 52427-791 — Duloxetine, 52427-821 — Duloxetine, 52427-913 — Duloxetine, 59651-279 — Duloxetine Hydrochloride, 59651-280 — Duloxetine Hydrochloride, 59651-282 — Duloxetine Hydrochloride, 60429-164 — 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.