NDC 31722-002 – Venlafaxine Hydrochloride

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

Human Prescription Drug

Product NDC31722-002

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine Hydrochloride
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212277
Marketed since
July 8, 2019
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 (4)

Package NDCDescriptionSince
31722-002-0110 BLISTER PACK in 1 CARTON (31722-002-01) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACKJul 8, 2019
31722-002-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-002-05)Jul 8, 2019
31722-002-3030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-002-30)Jul 8, 2019
31722-002-9090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-002-90)Jul 8, 2019

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