Paroxetine Hydrochloride NDC 62175-470

NDC codes

FDA NDC Directory

Product NDC (as listed)62175-470Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62175-0470Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
62175-470-32	62175047032	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-470-32)Marketed from Oct 31, 2014
62175-470-41	62175047041	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-470-41)Marketed from Oct 31, 2014

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Paroxetine Hydrochloride
Generic name (nonproprietary): paroxetine hydrochloride
Active ingredients: Paroxetine hydrochloride — 12.5 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: Lannett Company, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204744
Marketing start: Oct 31, 2014
Listing expires: Dec 31, 2026
Other FDA classes: Serotonin Uptake Inhibitors (Mechanism)
Identifiers: Product ID 62175-470_9474f942-d6d8-486b-8ea6-f8c561bb5014SPL ID 9474f942-d6d8-486b-8ea6-f8c561bb5014SPL set ID f22886f5-230c-47e4-9dd8-ffb14c8d6ae4RxCUI 1738803, 1738805, 1738807UNII X2ELS050D8UPC 0362175470324
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

N462175047032 followed by a unit qualifier and the quantity

Package 62175-0470-32. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 204744

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

FDA NDC Directory listings under ANDA 204744
Product	Strength	Form · route	Labeler	Product NDC
Paroxetine Hydrochloride	Paroxetine hydrochloride hemihydrate 25 mg/1	Tablet, Film coated, Extended releaseOral	Bryant Ranch Prepack	63629-8527
Paroxetine	Paroxetine hydrochloride 25 mg/1	Tablet, Film coated, Extended releaseOral	Chartwell RX, LLC	62135-426
Paroxetine	Paroxetine hydrochloride 12.5 mg/1	Tablet, Film coated, Extended releaseOral	Chartwell RX, LLC	62135-425
Paroxetine	Paroxetine hydrochloride 37.5 mg/1	Tablet, Film coated, Extended releaseOral	Chartwell RX, LLC	62135-427
Paroxetine Hydrochloride	Paroxetine hydrochloride 25 mg/1	Tablet, Film coated, Extended releaseOral	Lannett Company, Inc.	62175-471
Paroxetine Hydrochloride	Paroxetine hydrochloride 37.5 mg/1	Tablet, Film coated, Extended releaseOral	Lannett Company, Inc.	62175-472