NDC 70247-014 – Duloxetine

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

Human Prescription Drug

Product NDC70247-014

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Qingdao BAHEAL Pharmaceutical Co., Ltd.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA210599
Marketed since
May 5, 2018
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
70247-014-0330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-03)May 8, 2018
70247-014-0660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-06)May 8, 2018
70247-014-50500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-014-50)May 8, 2018

Other Duloxetine products