NDC 0615-8494 – Duloxetine

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

Human Prescription Drug

Product NDC0615-8494

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
December 11, 2013
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
0615-8494-3930 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8494-39)Jan 4, 2024

Other Duloxetine products