NDC 68382-021 – Venlafaxine

Venlafaxine Hydrochloride 75 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC68382-021

Product details

Brand name
Venlafaxine
Generic name
Venlafaxine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077653
Marketed since
June 13, 2008
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Venlafaxine →

Package NDC codes (6)

Package NDCDescriptionSince
68382-021-01100 TABLET in 1 BOTTLE (68382-021-01)Jun 13, 2008
68382-021-05500 TABLET in 1 BOTTLE (68382-021-05)Jun 13, 2008
68382-021-0630 TABLET in 1 BOTTLE (68382-021-06)Jun 13, 2008
68382-021-101000 TABLET in 1 BOTTLE (68382-021-10)Jun 13, 2008
68382-021-1460 TABLET in 1 BOTTLE (68382-021-14)Jun 13, 2008
68382-021-1690 TABLET in 1 BOTTLE (68382-021-16)Jun 13, 2008

Recalls mentioning this NDC

Other Venlafaxine products