NDC codes

FDA NDC Directory
Product NDC (as listed)24979-139Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24979-0139Add 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
24979-139-0124979013901100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (24979-139-01)Marketed from Aug 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)
Fluphenazine Hydrochloride
Generic name (nonproprietary)
fluphenazine hydrochloride
Active ingredients
Fluphenazine hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215848
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 24979-139_e2589baf-4d61-4d50-a578-41c51fbb6debSPL ID e2589baf-4d61-4d50-a578-41c51fbb6debSPL set ID d0a090fa-f7c9-4f6d-a9a3-9838870c7049RxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0324979139012, 0324979138015, 0324979137018, 0324979136011
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

N424979013901 followed by a unit qualifier and the quantity

Package 24979-0139-01. 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 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 215848

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

FDA NDC Directory listings under ANDA 215848
ProductStrengthForm · routeLabelerProduct NDC
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1Tablet, Film coatedOralProficient Rx LP71205-838
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralProficient Rx LP71205-839
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralProficient Rx LP71205-840
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralProficient Rx LP71205-837
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralUpsher-Smith Laboratories, LLC24979-136
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1Tablet, Film coatedOralUpsher-Smith Laboratories, LLC24979-137
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralUpsher-Smith Laboratories, LLC24979-138

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Fluphenazine Hydrochloride NDC 24979-139 | Med-Code