NDC 27241-099 – Duloxetine

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

Human Prescription Drug 3 recalls

Product NDC27241-099

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Ajanta Pharma 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 (3)

Package NDCDescriptionSince
27241-099-0330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-03)Mar 16, 2017
27241-099-4090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-40)Oct 18, 2021
27241-099-901000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (27241-099-90)Mar 16, 2017

Recalls mentioning this NDC

Other Duloxetine products