NDC 70518-1765 – Duloxetine

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

Human Prescription Drug

Product NDC70518-1765

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
January 2, 2019
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 (3)

Package NDCDescriptionSince
70518-1765-190 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-1)Jan 22, 2025
70518-1765-290 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1765-2)Jun 23, 2025
70518-1765-330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1765-3)Aug 8, 2025

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