NDC codes

FDA NDC Directory
Product NDC (as listed)62332-789Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62332-0789Add 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
62332-789-3162332078931100 TABLET, FILM COATED in 1 BOTTLE (62332-789-31)Marketed from Jul 25, 2024
62332-789-7162332078971500 TABLET, FILM COATED in 1 BOTTLE (62332-789-71)Marketed from Jul 25, 2024

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)
Fluphenazine Hydrochloride
Generic name (nonproprietary)
fluphenazine hydrochloride
Active ingredients
Fluphenazine hydrochloride — 2.5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218173
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 62332-789_f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4SPL ID f7ef2923-6d2a-4b1f-ad9c-c8127391b9f4SPL set ID 1991be2c-9629-4c3e-93f0-e40bcffc82b0RxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0362332790319, 0362332788316, 0362332789313, 0362332791316
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

N462332078931 followed by a unit qualifier and the quantity

Package 62332-0789-31. 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 Fluphenazine hydrochloride tablets are indicated in the management of manifestations of psychotic disorders. Fluphenazine hydrochloride has not been shown effective in 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 218173

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

FDA NDC Directory listings under ANDA 218173
ProductStrengthForm · routeLabelerProduct NDC
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralCoupler LLC67046-1547
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralCoupler LLC67046-1567
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-791
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-788
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Inc.62332-790
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-790
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-788
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-789
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-791

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