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Duloxetine

NDC 31722-168 · Camber Pharmaceuticals, Inc.

Generic nameDuloxetine
Dosage formCAPSULE, DELAYED RELEASE
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

31722-168-01 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-01)

31722-168-05 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-05)

31722-168-10 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-10)

31722-168-30 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-30)

31722-168-31 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (31722-168-31)

31722-168-32 105 CAPSULE, DELAYED RELEASE in 1 CARTON (31722-168-32)

31722-168-60 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-60)

31722-168-90 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (31722-168-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8494 — Duloxetine, 0615-8495 — Duloxetine, 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, 31722-169 — Duloxetine, 31722-170 — 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, +188 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels