NDC 68180-296 – Duloxetine

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

Human Prescription Drug 1 recall

Product NDC68180-296

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
December 11, 2013
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (3)

Package NDCDescriptionSince
68180-296-031000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-03)Dec 11, 2013
68180-296-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-06)Dec 11, 2013
68180-296-0990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-296-09)Jun 26, 2014

Recalls mentioning this NDC

Other Duloxetine products