NDC 68382-034 – Venlafaxine hydrochloride

Venlafaxine Hydrochloride 37.5 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug 3 recalls

Product NDC68382-034

Product details

Brand name
Venlafaxine hydrochloride
Generic name
Venlafaxine hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090174
Marketed since
June 1, 2011
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68382-034-0630 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-06)Jun 1, 2011
68382-034-101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10)Jun 1, 2011
68382-034-1690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-16)Jun 1, 2011

Recalls mentioning this NDC

Other Venlafaxine Hydrochloride products