NDC codes

FDA NDC Directory
Product NDC (as listed)63187-190Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0190Add 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
63187-190-306318701903030 TABLET, FILM COATED in 1 BOTTLE (63187-190-30)Marketed from Feb 2, 2015
63187-190-606318701906060 TABLET, FILM COATED in 1 BOTTLE (63187-190-60)Marketed from Feb 2, 2015
63187-190-906318701909090 TABLET, FILM COATED in 1 BOTTLE (63187-190-90)Marketed from Feb 2, 2015

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
Active ingredients
Paroxetine hydrochloride hemihydrate — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077584
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 63187-190_b0100eac-f51f-4aa9-88e1-f628aeea2412SPL ID b0100eac-f51f-4aa9-88e1-f628aeea2412SPL set ID 6318eefa-ee51-4e4e-91a5-8760d48bdc63RxCUI 1738483, 1738495, 1738511UNII X2ELS050D8
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

N463187019030 followed by a unit qualifier and the quantity

Package 63187-0190-30. 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)

INDICATIONS AND USAGE Major Depressive Disorder: Paroxetine tablets, USP are indicated for the treatment of major depressive disorder. The efficacy of paroxetine tablets, USP in the treatment of a major depressive episode was established in 6-week controlled trials of outpatients whose diagnoses corresponded most closely to the DSM-III category of major depressive disorder (see CLINICAL PHARMACOLOGY —Clinical Trials ). A major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should include at least 4 of the following 8 symptoms: Change in appetite, change in …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077584

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

FDA NDC Directory listings under ANDA 077584
ProductStrengthForm · routeLabelerProduct NDC
ParoxetineParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0321
ParoxetineParoxetine hydrochloride 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-6870
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-3349
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralCoupler LLC67046-0446
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc68788-0797
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-716
ParoxetineParoxetine hydrochloride hemihydrate 20 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-717
ParoxetineParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-718
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-719
ParoxetineParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-0850
ParoxetineParoxetine hydrochloride 30 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-7410
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralDirect_Rx72189-492
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralZydus Pharmaceuticals USA Inc.68382-001
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0544
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralDIRECT RX61919-513
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralProficient Rx LP63187-434
ParoxetineParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-2465
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3430
Paroxetineparoxetine hydrochlorideParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals, Inc68788-9074
ParoxetineParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralCoupler LLC67046-0846

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