NDC codes

FDA NDC Directory
Product NDC (as listed)23155-799Labeler and product segments. Claims need a package NDC.
Product NDC at billing width23155-0799Add 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
23155-799-012315507990123155079901100 TABLET in 1 BOTTLE (23155-799-01)Marketed from Oct 1, 2022

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)
Perphenazine
Generic name (nonproprietary)
perphenazine
Active ingredients
Perphenazine — 2 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210163
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 23155-799_4cc7f39f-fa21-4dc0-8ff7-5d6e5a7236a2SPL ID 4cc7f39f-fa21-4dc0-8ff7-5d6e5a7236a2SPL set ID 935a7567-0395-4901-960c-79587fa14c8dRxCUI 198075, 198076, 198077, 198078UNII FTA7XXY4EZUPC 0323155800012
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

N423155079901 followed by a unit qualifier and the quantity

Package 23155-0799-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE: Perphenazine is indicated for use in the treatment of schizophrenia and for the control of severe nausea and vomiting in adults. Perphenazine has not been shown effective for the management of behavioral complications in patients with mental retardation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-799

What is NDC 23155-799?
23155-799 is the product NDC for Perphenazine, Perphenazine 2 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Perphenazine.
What is the active ingredient?
Perphenazine.
Who is the labeler?
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Perphenazine?
72 other product NDCs are listed under this name. See all Perphenazine 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 Perphenazine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PerphenazinePerphenazine 2 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-468870518-4688-00
PerphenazinePerphenazine 16 mg/1TabletOralREMEDYREPACK INC.70518-448470518-4484-0070518-4484-02
PerphenazinePerphenazine 16 mg/1TabletOralREMEDYREPACK INC.70518-414470518-4144-00
PerphenazinePerphenazine 4 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-411270518-4112-00
PerphenazinePerphenazine 4 mg/1TabletOralMacleods Pharmaceuticals Limited33342-44933342-0449-1133342-0449-15
PerphenazinePerphenazine 2 mg/1TabletOralMacleods Pharmaceuticals Limited33342-44833342-0448-1133342-0448-15
PerphenazinePerphenazine 8 mg/1TabletOralMacleods Pharmaceuticals Limited33342-45033342-0450-1133342-0450-15
PerphenazinePerphenazine 16 mg/1TabletOralMacleods Pharmaceuticals Limited33342-45133342-0451-1133342-0451-15
PerphenazinePerphenazine 4 mg/1TabletOralChartwell RX, LLC62135-79962135-0799-90
PerphenazinePerphenazine 4 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-80023155-0800-01

All 73 Perphenazine NDCs

Other NDCs under ANDA 210163

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

FDA NDC Directory listings under ANDA 210163
ProductStrengthForm · routeLabelerProduct NDC
PerphenazinePerphenazine 4 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-800
PerphenazinePerphenazine 8 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-801
PerphenazinePerphenazine 16 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-802
PerphenazinePerphenazine 4 mg/1TabletOralChartwell RX, LLC62135-799
PerphenazinePerphenazine 16 mg/1TabletOralREMEDYREPACK INC.70518-4144

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