NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2398Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2398Add 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
72162-2398-172162239801100 TABLET, FILM COATED in 1 BOTTLE (72162-2398-1)Marketed from Sep 30, 2024
72162-2398-272162239802100 TABLET, FILM COATED in 1 BOTTLE (72162-2398-2)Marketed from Apr 30, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Perphenazine
Generic name (nonproprietary)
perphenazine
Active ingredients
Perphenazine — 8 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205973
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 72162-2398_07f0623c-5781-4ecd-b1aa-274504e9b16fSPL ID 07f0623c-5781-4ecd-b1aa-274504e9b16fSPL set ID f6af1fc3-868d-46f3-8bbe-828375fb0faeRxCUI 198078UNII FTA7XXY4EZ
Pharmacologic class
Phenothiazine

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

N472162239801 followed by a unit qualifier and the quantity

Package 72162-2398-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 205973

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

FDA NDC Directory listings under ANDA 205973
ProductStrengthForm · routeLabelerProduct NDC
PerphenazinePerphenazine 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2893
PerphenazinePerphenazine 4 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1125
PerphenazinePerphenazine 16 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1109
PerphenazinePerphenazine 8 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-1133
PerphenazinePerphenazine 2 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2396
PerphenazinePerphenazine 4 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2397
PerphenazinePerphenazine 16 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2399
PerphenazinePerphenazine 8 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-168
PerphenazinePerphenazine 2 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-162
PerphenazinePerphenazine 4 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-164
PerphenazinePerphenazine 16 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-170

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