NDC 67877-265 – Duloxetine

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

Human Prescription Drug

Product NDC67877-265

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Ascend Laboratories, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203197
Marketed since
May 1, 2012
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (4)

Package NDCDescriptionSince
67877-265-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-01)May 1, 2012
67877-265-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-10)May 1, 2012
67877-265-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-30)May 1, 2012
67877-265-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-265-90)May 1, 2012

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