NDC codes

FDA NDC Directory
Product NDC (as listed)71610-204Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0204Add 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
71610-204-607161002046090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-204-60)Marketed from Dec 13, 2018

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 — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
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 71610-204_127e7f93-615c-45d1-91a6-98091c1e2d81SPL ID 127e7f93-615c-45d1-91a6-98091c1e2d81SPL set ID 2eebd2b6-7c64-45ca-8eb5-5201137f610aRxCUI 1738483UNII 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

N471610020460 followed by a unit qualifier and the quantity

Package 71610-0204-60. 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 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 40 mg/1Tablet, Film coatedOralMylan Pharmaceuticals Inc.0378-7004
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 20 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8777
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 40 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC43353-544
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 20 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC43353-554
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 10 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.55289-037
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.55289-053
Paroxetineparoxetine hydrochloride hemihydrateParoxetine hydrochloride hemihydrate 30 mg/1Tablet, Film coatedOralAphena Pharma Solutions - Tennessee, LLC71610-243
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

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