NDC 68788-8825 – Venlafaxine Hydrochloride

Venlafaxine Hydrochloride 75 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC68788-8825

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA216044
Marketed since
February 10, 2025
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
68788-8825-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-3)Feb 10, 2025
68788-8825-660 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-6)Feb 10, 2025
68788-8825-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-9)Feb 10, 2025

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