NDC 70710-1348 – Venlafaxine

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

Human Prescription Drug

Product NDC70710-1348

Product details

Brand name
Venlafaxine
Generic name
Venlafaxine
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215622
Marketed since
September 1, 2022
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 (3)

Package NDCDescriptionSince
70710-1348-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-1)Sep 1, 2022
70710-1348-330 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-3)Sep 1, 2022
70710-1348-990 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1348-9)Sep 1, 2022

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