NDC 27241-221 – Venlafaxine

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

Human Prescription Drug

Product NDC27241-221

Product details

Brand name
Venlafaxine
Generic name
Venlafaxine
Labeler
Ajanta Pharma USA Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214691
Marketed since
April 12, 2023
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 (2)

Package NDCDescriptionSince
27241-221-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-221-30)Apr 12, 2023
27241-221-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (27241-221-90)Apr 12, 2023

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