NDC 68001-570 – Duloxetine

Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68001-570

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
BluePoint Laboratories
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
July 28, 2023
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
68001-570-0430 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-570-04)Jul 28, 2023

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