NDC codes

FDA NDC Directory
Product NDC (as listed)27241-254Labeler and product segments. Claims need a package NDC.
Product NDC at billing width27241-0254Add 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
27241-254-012724102540127241025401100 TABLET in 1 BOTTLE (27241-254-01)Marketed from Jan 5, 2023

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
Route
Oral
Labeler
Ajanta Pharma USA Inc.NDC labeler code 27241
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217410
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 27241-254_0069bda4-a743-4edd-a15f-a53cba1a2bffSPL ID 0069bda4-a743-4edd-a15f-a53cba1a2bffSPL set ID 47695e20-9c0b-4a6b-ab1a-1dfaa75e96d8RxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0327241255014, 0327241252013, 0327241253010, 0327241254017
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

N427241025401 followed by a unit qualifier and the quantity

Package 27241-0254-01. 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, USP are indicated in the management of manifestations of psychotic disorders. Fluphenazine hydrochloride USP 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)

About NDC 27241-254

What is NDC 27241-254?
27241-254 is the product NDC for Fluphenazine hydrochloride, Fluphenazine hydrochloride 2.5 mg/1 tablet, listed with the FDA by Ajanta Pharma USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fluphenazine hydrochloride.
What is the active ingredient?
Fluphenazine hydrochloride.
Who is the labeler?
Ajanta Pharma USA Inc., NDC labeler code 27241. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fluphenazine hydrochloride?
99 other product NDCs are listed under this name. See all Fluphenazine hydrochloride 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 Fluphenazine hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
fluphenazine hydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralCoupler LLC67046-097567046-0975-03
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-467370518-4673-00
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-38431722-0384-0131722-0384-05
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-38531722-0385-0131722-0385-05
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-38631722-0386-0131722-0386-05
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-38731722-0387-0131722-0387-05
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralCoupler LLC67046-156767046-1567-03
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1Tablet, Film coatedOralCoupler LLC67046-154767046-1547-03
Fluphenazine hydrochlorideFluphenazine hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-427370518-4273-0070518-4273-01
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1Tablet, Film coatedOralAlembic Pharmaceuticals Limited46708-78846708-0788-3146708-0788-71

All 100 Fluphenazine hydrochloride NDCs

Other NDCs under ANDA 217410

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

FDA NDC Directory listings under ANDA 217410
ProductStrengthForm · routeLabelerProduct NDC
Fluphenazine hydrochlorideFluphenazine hydrochloride 10 mg/1TabletOralAjanta Pharma USA Inc.27241-252
Fluphenazine hydrochlorideFluphenazine hydrochloride 5 mg/1TabletOralAjanta Pharma USA Inc.27241-253
Fluphenazine hydrochlorideFluphenazine hydrochloride 1 mg/1TabletOralAjanta Pharma USA Inc.27241-255
Fluphenazine hydrochlorideFluphenazine hydrochloride 5 mg/1TabletOralREMEDYREPACK INC.70518-4273

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