Drug Atlas

NDC 68382-609 – Trazodone Hydrochloride

Trazodone Hydrochloride 50 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68382-609

Product details

Brand name: Trazodone Hydrochloride
Generic name: Trazodone Hydrochloride
Labeler: Zydus Pharmaceuticals USA Inc.
Dosage form: Tablet
Route: Oral
Marketing category: ANDA · ANDA205253
Marketed since: January 22, 2026
Listing expires: December 31, 2027
Pharmacologic class: Serotonin Reuptake Inhibitor

Active ingredients

Trazodone Hydrochloride 50 mg/1

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

Package NDC codes (3)

Package NDC	Description	Since
68382-609-01	100 TABLET in 1 BOTTLE (68382-609-01)	Jan 22, 2026
68382-609-05	500 TABLET in 1 BOTTLE (68382-609-05)	Jan 22, 2026
68382-609-10	1000 TABLET in 1 BOTTLE (68382-609-10)	Jan 22, 2026

Recalls mentioning this NDC

D-0247-2026 Jan 7, 2026 · Class III
Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface.

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