NDC 68382-808 – Trazodone Hydrochloride

Trazodone Hydrochloride 300 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC68382-808

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
December 11, 2017
Listing expires
December 31, 2027
Pharmacologic class
Serotonin Reuptake Inhibitor

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
68382-808-01100 TABLET in 1 BOTTLE (68382-808-01)Dec 11, 2017
68382-808-05500 TABLET in 1 BOTTLE (68382-808-05)Dec 11, 2017
68382-808-0630 TABLET in 1 BOTTLE (68382-808-06)Dec 11, 2017
68382-808-101000 TABLET in 1 BOTTLE (68382-808-10)Dec 11, 2017
68382-808-1690 TABLET in 1 BOTTLE (68382-808-16)Dec 11, 2017
68382-808-7710 BLISTER PACK in 1 CARTON (68382-808-77) / 10 TABLET in 1 BLISTER PACK (68382-808-30)Dec 11, 2017

Recalls mentioning this NDC

Other Trazodone Hydrochloride products