NDC 70518-0122 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC70518-0122

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
January 13, 2017
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 (1)

Package NDCDescriptionSince
70518-0122-590 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-0122-5)Oct 2, 2024

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