NDC 68180-297 – Duloxetine

Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC68180-297

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
May 25, 2015
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 (1)

Package NDCDescriptionSince
68180-297-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-297-06)Jul 15, 2015

Recalls mentioning this NDC

Other Duloxetine products