NDC 76420-633 – Duloxetine

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC76420-633

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Asclemed USA, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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 (7)

Package NDCDescriptionSince
76420-633-001000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-00)Apr 3, 2025
76420-633-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-01)Oct 17, 2023
76420-633-05500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-05)Apr 3, 2025
76420-633-2020 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-20)Apr 3, 2025
76420-633-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-30)Oct 17, 2023
76420-633-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-60)Oct 17, 2023
76420-633-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-633-90)Oct 17, 2023

Recalls mentioning this NDC

Other Duloxetine products