NDC 43598-002 – Venlafaxine hydrochloride

Venlafaxine Hydrochloride 150 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC43598-002

Product details

Brand name
Venlafaxine hydrochloride
Generic name
Venlafaxine hydrochloride
Labeler
Dr.Reddys Laboratories Inc
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078421
Marketed since
September 9, 2024
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
43598-002-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-05)Sep 9, 2024
43598-002-3030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-30)Sep 9, 2024
43598-002-9090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (43598-002-90)Sep 9, 2024

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