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DRIZALMA SPRINKLE

NDC 47335-619 · SUN PHARMACEUTICAL INDUSTRIES, INC.

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 categoryNDA

Packages

47335-619-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-10)

47335-619-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-30)

47335-619-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-60)

47335-619-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (47335-619-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-381 — Duloxetine, 46708-278 — Duloxetine, 46708-279 — Duloxetine, 46708-280 — Duloxetine, 47335-381 — Duloxetine, 47335-382 — Duloxetine, 47335-383 — Duloxetine, 47335-616 — Duloxetine, 47335-617 — Duloxetine, 47335-618 — Duloxetine, 49252-007 — duloxetine, 49252-008 — duloxetine, 49252-009 — duloxetine, 50090-3205 — DULOXETINE HYDROCHLORIDE, 50090-5940 — Duloxetine, 50090-6281 — Duloxetine, 50090-6406 — Duloxetine, 50090-6775 — Duloxetine, 50090-6889 — DULOXETINE HYDROCHLORIDE, 50090-6893 — 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.