NDC codes

FDA NDC Directory
Product NDC (as listed)52536-162Labeler and product segments. Claims need a package NDC.
Product NDC at billing width52536-0162Add 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
52536-162-0152536016201100 TABLET, FILM COATED in 1 BOTTLE (52536-162-01)Marketed from Feb 6, 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)
Perphenazine
Generic name (nonproprietary)
perphenazine
Active ingredients
Perphenazine — 2 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 52536-162_325b0584-e6f3-f087-e063-6394a90a64c5SPL ID 325b0584-e6f3-f087-e063-6394a90a64c5SPL set ID 5e455842-4892-4795-8c9b-4109a8f30783RxCUI 198075, 198076, 198077, 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

N452536016201 followed by a unit qualifier and the quantity

Package 52536-0162-01. 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)

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 8 mg/1Tablet, Film coatedOralBryant Ranch Prepack72162-2398
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 4 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-164
PerphenazinePerphenazine 16 mg/1Tablet, Film coatedOralWilshire Pharmaceuticals, Inc.52536-170

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