NDC 68180-295 – Duloxetine

Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug 1 recall

Product NDC68180-295

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
68180-295-031000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-03)Mar 6, 2014
68180-295-0630 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-06)Dec 11, 2013
68180-295-0990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-09)Dec 11, 2013

Recalls mentioning this NDC

Other Duloxetine products