NDC codes

FDA NDC Directory
Product NDC (as listed)60429-734Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60429-0734Add 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 NDC11-digit (billing)PackageCopy
60429-734-10604290734101000 TABLET, FILM COATED in 1 BOTTLE (60429-734-10)Marketed from Jan 1, 2019
60429-734-306042907343030 TABLET, FILM COATED in 1 BOTTLE (60429-734-30)Marketed from Jan 1, 2019
60429-734-906042907349090 TABLET, FILM COATED in 1 BOTTLE (60429-734-90)Marketed from Jan 1, 2019

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
Generic name (nonproprietary)
paroxetine hydrochloride
Active ingredients
Paroxetine hydrochloride anhydrous — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 075356
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 60429-734_52d4a27a-f543-6e04-e063-6394a90afc87SPL ID 52d4a27a-f543-6e04-e063-6394a90afc87SPL set ID e63fe922-b35a-406c-8737-f3f5e6d5a30dRxCUI 1738483, 1738495, 1738503, 1738511UNII 3I3T11UD2S
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

N460429073410 followed by a unit qualifier and the quantity

Package 60429-0734-10. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

Paroxetine tablets are indicated in adults for the treatment of: Major depressive disorder (MDD) Obsessive compulsive disorder (OCD) Panic disorder (PD) Social anxiety disorder (SAD) Generalized anxiety disorder (GAD) Posttraumatic stress disorder (PTSD) Paroxetine tablets is a selective serotonin reuptake inhibitor (SSRI) indicated in adults for the treatment of ( 1 ): Major Depressive Disorder (MDD) Obsessive Compulsive Disorder (OCD) Panic Disorder (PD) Social Anxiety Disorder (SAD) Generalized Anxiety Disorder (GAD) Posttraumatic Stress Disorder (PTSD)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 075356

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

FDA NDC Directory listings under ANDA 075356
ProductStrengthForm · routeLabelerProduct NDC
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-7999
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 40 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-0993
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 40 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-737
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-735
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 30 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-736
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 10 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-5676
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 30 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1460
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-5677
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralApotex Corp.60505-0083
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 30 mg/1Tablet, Film coatedOralApotex Corp.60505-0084
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 40 mg/1Tablet, Film coatedOralApotex Corp.60505-0101
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 10 mg/1Tablet, Film coatedOralApotex Corp.60505-0097
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC67544-317
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 40 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC67544-492
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 20 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2871
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride anhydrous 40 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-992

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