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Duloxetine

NDC 31722-170 · Camber Pharmaceuticals, 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 categoryANDA

Packages

31722-170-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-01)

31722-170-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-10)

31722-170-30 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-30)

31722-170-31 — 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-170-31)

31722-170-90 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-170-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8496 — Duloxetine, 25000-608 — Duloxetine Hydrochloride, 25000-609 — Duloxetine Hydrochloride, 25000-610 — Duloxetine Hydrochloride, 27241-097 — Duloxetine, 27241-098 — Duloxetine, 27241-099 — Duloxetine, 27241-164 — Duloxetine, 31722-168 — Duloxetine, 31722-169 — Duloxetine, 33342-160 — Duloxetine Hydrochloride, 33342-161 — Duloxetine Hydrochloride, 33342-162 — Duloxetine Hydrochloride, 42708-196 — Duloxetine, 43547-379 — Duloxetine, 43547-380 — Duloxetine, 43547-381 — Duloxetine, 46708-278 — Duloxetine, 46708-279 — Duloxetine, 46708-280 — 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.