NDC 52427-821 – Duloxetine

Duloxetine Hydrochloride 80 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC52427-821

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Almatica Pharma LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
NDA · NDA219131
Marketed since
July 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (1)

Package NDCDescriptionSince
52427-821-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (52427-821-30)Jul 1, 2026

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