NDC 70518-1011 – Duloxetine

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

Human Prescription Drug

Product NDC70518-1011

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
REMEDYREPACK INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
February 12, 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 (3)

Package NDCDescriptionSince
70518-1011-030 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-1011-0)Feb 12, 2018
70518-1011-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-1)Apr 17, 2019
70518-1011-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1011-2)May 4, 2020

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