NDC 67877-264 – Duloxetine

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

Human Prescription Drug

Product NDC67877-264

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
67877-264-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-01)May 1, 2012
67877-264-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-10)May 1, 2012
67877-264-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-30)May 1, 2012
67877-264-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-264-90)May 1, 2012

Other Duloxetine products