NDC 71610-954 – Duloxetine

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

Human Prescription Drug

Product NDC71610-954

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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 (3)

Package NDCDescriptionSince
71610-954-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-30)Oct 14, 2025
71610-954-5360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-53)Oct 14, 2025
71610-954-6090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-954-60)Oct 14, 2025

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