Paroxetine (paroxetine hydrochloride) NDC 60505-0084

Product information

Brand name (proprietary)

Paroxetine

Generic name (nonproprietary)

paroxetine hydrochloride

Active ingredients

Paroxetine hydrochloride anhydrous — 30 mg/1

Dosage form

Tablet, Film coated

Route

Oral

Labeler

Apotex Corp.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 075356

Marketing start

Sep 8, 2003

Listing expires

Dec 31, 2027

Other FDA classes

Serotonin Uptake Inhibitors (Mechanism)

Identifiers

Product ID 60505-0084_372affaa-7ff0-8369-d124-358a79da4bbeSPL ID 372affaa-7ff0-8369-d124-358a79da4bbe

Pharmacologic class

Serotonin 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

N460505008401 followed by a unit qualifier and the quantity Copy

Package 60505-0084-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 075356

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