NDC 67046-1451 – Duloxetine

Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC67046-1451

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Coupler LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
February 7, 2025
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (1)

Package NDCDescriptionSince
67046-1451-330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (67046-1451-3)Feb 7, 2025

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