NDC 82009-170 – Duloxetine

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC82009-170

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
July 1, 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
82009-170-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-170-10)Jul 1, 2025

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