NDC 0002-3270 – Cymbalta

Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC0002-3270

Product details

Brand name
Cymbalta
Generic name
Duloxetine hydrochloride
Labeler
Eli Lilly and Company
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
NDA · NDA021427
Marketed since
January 15, 2010
Marketing end
October 2, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Cymbalta →

Package NDC codes (0)

Package NDCDescriptionSince

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