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Cymbalta

NDC 0002-3235 · Eli Lilly and Company

Generic nameDuloxetine hydrochloride
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 categoryNDA

Packages

0002-3235-60 — 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0002-3235-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0002-3240 — Duloxetine hydrochloride, 0002-3270 — Duloxetine hydrochloride, 0228-2890 — Duloxetine, 0228-2891 — Duloxetine, 0228-2892 — Duloxetine, 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, 31722-168 — Duloxetine, 31722-169 — Duloxetine, 31722-170 — Duloxetine, 33342-160 — Duloxetine Hydrochloride, 33342-161 — 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.

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