Venlafaxine Hydrochloride NDC 71335-2779

Product information

Brand name (proprietary)

Venlafaxine Hydrochloride

Generic name (nonproprietary)

venlafaxine hydrochloride

Active ingredients

Venlafaxine hydrochloride — 37.5 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 217390

Marketing start

Sep 25, 2023

Listing expires

Dec 31, 2027

Other FDA classes

Norepinephrine Uptake Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 71335-2779_d62baf0c-d78e-42b3-9739-93cb3dcafc53SPL ID d62baf0c-d78e-42b3-9739-93cb3dcafc53SPL set ID 7aa3edba-4248-49bb-86f7-06fdbf2a6fb7RxCUI 313583UNII 7D7RX5A8MO

Pharmacologic class

Serotonin and Norepinephrine Reuptake Inhibitor

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335277901 followed by a unit qualifier and the quantity Copy

Package 71335-2779-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Other NDCs under ANDA 217390

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.