NDC 65841-801 – Duloxetine

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

Human Prescription Drug

Product NDC65841-801

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Zydus Lifesciences Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090739
Marketed since
May 27, 2014
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 (3)

Package NDCDescriptionSince
65841-801-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-06)May 27, 2014
65841-801-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-10)May 27, 2014
65841-801-1690 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-801-16)May 27, 2014

Other Duloxetine products