NDC 70518-1244 – Duloxetine

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

Human Prescription Drug

Product NDC70518-1244

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
June 5, 2018
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 (7)

Package NDCDescriptionSince
70518-1244-030 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-0)Jun 5, 2018
70518-1244-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-1)Mar 24, 2025
70518-1244-330 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1244-3)Dec 9, 2025
70518-1244-450 POUCH in 1 BOX (70518-1244-4) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-5)May 17, 2026
70518-1244-650 POUCH in 1 BOX (70518-1244-6) / 1 CAPSULE, DELAYED RELEASE in 1 POUCH (70518-1244-7)Jul 6, 2026
70518-1244-890 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-8)Aug 5, 2026
70518-1244-930 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1244-9)Aug 10, 2026

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