NDC codes

FDA NDC Directory
Product NDC (as listed)43353-544Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43353-0544Add 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
43353-544-15433530544154335305441515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-544-15)Marketed from Sep 21, 2009
43353-544-30433530544304335305443030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-544-30)Marketed from Feb 1, 2019
43353-544-45433530544454335305444545 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-544-45)Marketed from Jan 12, 2010
43353-544-60433530544604335305446090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43353-544-60)Marketed from Mar 18, 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 hemihydrate
Active ingredients
Paroxetine hydrochloride hemihydrate — 40 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 43353
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078902
Marketing start
Listing expires
Other FDA classes
Serotonin Uptake Inhibitors (Mechanism)
Identifiers
Product ID 43353-544_37d67ac2-1470-43aa-a06d-b24981539fd4SPL ID 37d67ac2-1470-43aa-a06d-b24981539fd4SPL set ID ec9622ca-1f56-4216-9445-485791c4c0edRxCUI 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

N443353054415 followed by a unit qualifier and the quantity

Package 43353-0544-15. 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 are indicated for the treatment of major depressive disorder. The efficacy of paroxetine tablets 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 four of the following eight symptoms: Change in appetite, change in slee…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43353-544

What is NDC 43353-544?
43353-544 is the product NDC for Paroxetine (paroxetine hydrochloride hemihydrate), Paroxetine hydrochloride hemihydrate 40 mg/1 tablet, film coated, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Paroxetine (Paroxetine hydrochloride hemihydrate).
What is the active ingredient?
Paroxetine hydrochloride hemihydrate.
Who is the labeler?
Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 43353. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Paroxetine?
145 other product NDCs are listed under this name. See all Paroxetine NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Paroxetine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-413068788-4130-0168788-4130-0368788-4130-06+2 more
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralCoupler LLC67046-044667046-0446-03
ParoxetineParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralCoupler LLC67046-084667046-0846-03
ParoxetineParoxetine hydrochloride hemihydrate 12.5 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Limited46708-76646708-0766-3046708-0766-91
ParoxetineParoxetine hydrochloride hemihydrate 12.5 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Inc.62332-76662332-0766-3062332-0766-91
ParoxetineParoxetine hydrochloride hemihydrate 25 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Limited46708-76746708-0767-3046708-0767-91
ParoxetineParoxetine hydrochloride hemihydrate 37.5 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Limited46708-76846708-0768-3046708-0768-91
ParoxetineParoxetine hydrochloride hemihydrate 25 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Inc.62332-76762332-0767-3062332-0767-91
ParoxetineParoxetine hydrochloride hemihydrate 37.5 mg/1Tablet, Film coated, Extended releaseOralAlembic Pharmaceuticals Inc.62332-76862332-0768-3062332-0768-91
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-882968788-8829-0168788-8829-0368788-8829-06+2 more

All 146 Paroxetine NDCs

Other NDCs under ANDA 078902

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

FDA NDC Directory listings under ANDA 078902
ProductStrengthForm · routeLabelerProduct NDC
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 20 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC43353-554
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8777
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.55289-053
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.55289-037
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-7001
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-7002
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 30 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-7003
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-204
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 40 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-7004
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-243

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