NDC codes

FDA NDC Directory
Product NDC (as listed)70954-273Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70954-0273Add 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
70954-273-107095402731070954027310100 TABLET in 1 BOTTLE (70954-273-10)Marketed from Mar 1, 2021

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 — 1 mg/1
Dosage form
Tablet
Route
Oral
Labeler
ANI Pharmaceuticals, Inc.NDC labeler code 70954
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214674
Marketing start
Listing expires
Other FDA classes
Phenothiazines (Chemical structure)
Identifiers
Product ID 70954-273_b62e66ce-9c80-46f1-bb86-68f7f73c487cSPL ID b62e66ce-9c80-46f1-bb86-68f7f73c487cSPL set ID 6218cbd2-1f7f-40fa-92d2-5d5b0d7fa60bRxCUI 859841, 860918, 865117, 865123UNII ZOU145W1XLUPC 0370954275107, 0370954276104, 0370954276203, 0370954275206, 0370954273103
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

N470954027310 followed by a unit qualifier and the quantity

Package 70954-0273-10. 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 & 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)

About NDC 70954-273

What is NDC 70954-273?
70954-273 is the product NDC for Fluphenazine Hydrochloride, Fluphenazine hydrochloride 1 mg/1 tablet, listed with the FDA by ANI Pharmaceuticals, 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?
ANI Pharmaceuticals, Inc., NDC labeler code 70954. 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 214674

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

FDA NDC Directory listings under ANDA 214674
ProductStrengthForm · routeLabelerProduct NDC
Fluphenazine HydrochlorideFluphenazine hydrochloride 1 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-725
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-726
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-727
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1TabletOralMarlex Pharmaceuticals, Inc.10135-728
Fluphenazine HydrochlorideFluphenazine hydrochloride 2.5 mg/1TabletOralANI Pharmaceuticals, Inc.70954-274
Fluphenazine HydrochlorideFluphenazine hydrochloride 5 mg/1TabletOralANI Pharmaceuticals, Inc.70954-275
Fluphenazine HydrochlorideFluphenazine hydrochloride 10 mg/1TabletOralANI Pharmaceuticals, Inc.70954-276

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