NDC 70518-2630 – Duloxetine

Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC70518-2630

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2020
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (2)

Package NDCDescriptionSince
70518-2630-290 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-2)Jul 28, 2020
70518-2630-3180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2630-3)Oct 9, 2025

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