NDC 70518-3287 – Duloxetine

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

Human Prescription Drug

Product NDC70518-3287

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
December 9, 2021
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 (5)

Package NDCDescriptionSince
70518-3287-060 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-0)Dec 9, 2021
70518-3287-290 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3287-2)May 28, 2025
70518-3287-350 POUCH in 1 BOX (70518-3287-3) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-3287-4)Apr 23, 2026
70518-3287-550 POUCH in 1 BOX (70518-3287-5) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-3287-6)May 15, 2026
70518-3287-750 POUCH in 1 BOX (70518-3287-7) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-3287-8)Sep 4, 2026

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