NDC codes

FDA NDC Directory
Product NDC (as listed)51407-695Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51407-0695Add 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
51407-695-0151407069501100 TABLET in 1 BOTTLE (51407-695-01)Marketed from Dec 21, 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 — 4 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205232
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 51407-695_29f7902b-4fd6-8122-e063-6294a90a13a0SPL ID 29f7902b-4fd6-8122-e063-6294a90a13a0SPL set ID f0ea4d18-643d-7acb-e053-2a95a90a9ea7RxCUI 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

N451407069501 followed by a unit qualifier and the quantity

Package 51407-0695-01. 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 tablets, USP are indicated for use in the treatment of schizophrenia and for the control of severe nausea and vomiting in adults. Perphenazine tablets, USP have 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 205232

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

FDA NDC Directory listings under ANDA 205232
ProductStrengthForm · routeLabelerProduct NDC
perphenazinePerphenazine 8 mg/1TabletOralZydus Lifesciences Limited70771-1043
perphenazinePerphenazine 2 mg/1TabletOralZydus Lifesciences Limited70771-1041
perphenazinePerphenazine 4 mg/1TabletOralZydus Lifesciences Limited70771-1042
perphenazinePerphenazine 16 mg/1TabletOralZydus Lifesciences Limited70771-1044
perphenazinePerphenazine 4 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.68382-592
perphenazinePerphenazine 2 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.68382-591
perphenazinePerphenazine 2 mg/1TabletOralGolden State Medical Supply, Inc.51407-694
perphenazinePerphenazine 8 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.68382-593
perphenazinePerphenazine 16 mg/1TabletOralZydus Pharmaceuticals (USA) Inc.68382-594
perphenazinePerphenazine 16 mg/1TabletOralGolden State Medical Supply, Inc.51407-697
perphenazinePerphenazine 8 mg/1TabletOralGolden State Medical Supply, Inc.51407-696
perphenazinePerphenazine 2 mg/1TabletOralREMEDYREPACK INC.70518-3257

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