venlafaxine hydrochloride NDC 65841-752

Product information

Brand name (proprietary)

venlafaxine hydrochloride

Generic name (nonproprietary)

venlafaxine hydrochloride

Active ingredients

Venlafaxine hydrochloride — 75 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Zydus Lifesciences Limited

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 090174

Marketing start

Jun 1, 2011

Listing expires

Dec 31, 2026

Other FDA classes

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

Identifiers

Product ID 65841-752_f20749dc-d1f6-4860-b583-82b82d3a2242SPL ID f20749dc-d1f6-4860-b583-82b82d3a2242SPL set ID 1be1be3a-304b-4e31-8732-335247029191RxCUI 313581, 313583, 313585UNII 7D7RX5A8MOUPC 0365841752106, 0365841753103

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

N465841075206 followed by a unit qualifier and the quantity Copy

Package 65841-0752-06. 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 090174

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