NDC codes

FDA NDC Directory
Product NDC (as listed)65841-099Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65841-0099Add 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
65841-099-016584100990165841009901100 TABLET, FILM COATED in 1 BOTTLE (65841-099-01)Marketed from Apr 13, 2007
65841-099-056584100990565841009905500 TABLET, FILM COATED in 1 BOTTLE (65841-099-05)Marketed from Apr 13, 2007
65841-099-06658410099066584100990630 TABLET, FILM COATED in 1 BOTTLE (65841-099-06)Marketed from Apr 13, 2007
65841-099-1065841009910658410099101000 TABLET, FILM COATED in 1 BOTTLE (65841-099-10)Marketed from Apr 13, 2007
65841-099-16658410099166584100991690 TABLET, FILM COATED in 1 BOTTLE (65841-099-16)Marketed from Apr 13, 2007

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 — 30 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Zydus Lifesciences LimitedNDC labeler code 65841
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 65841-099_ef5c1ef5-2884-4395-a65a-92591c986150SPL ID ef5c1ef5-2884-4395-a65a-92591c986150SPL set ID 6d5fcdb2-4d84-4b20-87e3-58a43e567500RxCUI 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

N465841009901 followed by a unit qualifier and the quantity

Package 65841-0099-01. 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

Current FDA label (SPL), effective .

Full label on DailyMed (opens in a new tab)

About NDC 65841-099

What is NDC 65841-099?
65841-099 is the product NDC for Paroxetine (paroxetine hydrochloride), Paroxetine hydrochloride anhydrous 30 mg/1 tablet, film coated, listed with the FDA by Zydus Lifesciences Limited. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Paroxetine (Paroxetine Hydrochloride).
What is the active ingredient?
Paroxetine hydrochloride anhydrous.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 65841. 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 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 10 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-044
ParoxetineParoxetine hydrochloride 40 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-6870
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-1740
ParoxetineParoxetine hydrochloride hemihydrate 10 mg/1Tablet, Film coatedOralProficient Rx LP63187-190
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-3349
ParoxetineParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-0850
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 30 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-0321
ParoxetineParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-719
ParoxetineParoxetine hydrochloride 30 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-7410
ParoxetineParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-1297
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 20 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-045
ParoxetineParoxetine hydrochloride 30 mg/1Tablet, Film coatedOralAmerican Health Packaging68084-046

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