NDC 0591-3660 – Desvenlafaxine

Desvenlafaxine Succinate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC0591-3660

Product details

Brand name
Desvenlafaxine
Generic name
Desvenlafaxine
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA204065
Marketed since
March 1, 2017
Marketing end
January 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Desvenlafaxine →

Package NDC codes (1)

Package NDCDescriptionSince
0591-3660-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-3660-30)Mar 1, 2017

Recalls mentioning this NDC

Other Desvenlafaxine products