NDC 50111-561 – Trazodone Hydrochloride

Trazodone Hydrochloride 100 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC50111-561

Product details

Brand name
Trazodone Hydrochloride
Generic name
Trazodone Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA071524
Marketed since
October 8, 2020
Listing expires
December 31, 2026
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Trazodone Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
50111-561-01100 TABLET in 1 BOTTLE (50111-561-01)Dec 8, 2020
50111-561-02500 TABLET in 1 BOTTLE (50111-561-02)Dec 8, 2020
50111-561-031000 TABLET in 1 BOTTLE (50111-561-03)Oct 8, 2020

Recalls mentioning this NDC

Other Trazodone Hydrochloride products