NDC codes

FDA NDC Directory
Product NDC (as listed)72189-456Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0456Add 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
72189-456-307218904563030 TABLET in 1 BOTTLE (72189-456-30)Marketed from Mar 30, 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)
Aripiprazole
Generic name (nonproprietary)
aripiprazole
Active ingredients
Aripiprazole — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_RxNDC labeler code 72189
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205064
Marketing start
Listing expires
Identifiers
Product ID 72189-456_2c4dbb36-483f-f211-e063-6294a90ad364SPL ID 2c4dbb36-483f-f211-e063-6294a90ad364SPL set ID f823bc23-27f3-2397-e053-6294a90a365aRxCUI 402131UNII 82VFR53I78
Pharmacologic class
Atypical Antipsychotic

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

N472189045630 followed by a unit qualifier and the quantity

Package 72189-0456-30. 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)

Aripiprazole oral tablets are indicated for the treatment of: • Schizophrenia [see Clinical Studies ( 14.1)] Additional pediatric use information is approved for Otsuka America Pharmaceutical, Inc.’s ABILIFY ® (aripiprazole) product. However, due to Otsuka America Pharmaceutical, Inc.’s marketing exclusivity rights, this drug product is not labeled with that information.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-456

What is NDC 72189-456?
72189-456 is the product NDC for Aripiprazole, Aripiprazole 5 mg/1 tablet, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Aripiprazole.
What is the active ingredient?
Aripiprazole.
Who is the labeler?
Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aripiprazole?
256 other product NDCs are listed under this name. See all Aripiprazole 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 Aripiprazole NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AripiprazoleAripiprazole 15 mg/1TabletOralREMEDYREPACK INC.70518-474570518-4745-00
AripiprazoleAripiprazole 10 mg/1TabletOralCoupler LLC67046-087367046-0873-03
AripiprazoleAripiprazole 15 mg/1TabletOralCoupler LLC67046-204667046-2046-03
AripiprazoleAripiprazole 2 mg/1TabletOralCoupler LLC67046-105267046-1052-03
AripiprazoleAripiprazole 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-00687441-0006-01
AripiprazoleAripiprazole 20 mg/1TabletOralCoupler LLC67046-108567046-1085-03
AripiprazoleAripiprazole 5 mg/1TabletOralCoupler LLC67046-088567046-0885-03
AripiprazoleAripiprazole 15 mg/1TabletOralCoupler LLC67046-101767046-1017-03
AripiprazoleAripiprazole 10 mg/1TabletOralCoupler LLC67046-049267046-0492-03
AripiprazoleAripiprazole 10 mg/1Tablet, Orally disintegratingOralAurobindo Pharma Limited59651-51459651-0514-0359651-0514-30

All 257 Aripiprazole NDCs

Other NDCs under ANDA 205064

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

FDA NDC Directory listings under ANDA 205064
ProductStrengthForm · routeLabelerProduct NDC
AripiprazoleAripiprazole 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-462
AripiprazoleAripiprazole 2 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-044
AripiprazoleAripiprazole 5 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-045
AripiprazoleAripiprazole 10 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-046
AripiprazoleAripiprazole 15 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-047
AripiprazoleAripiprazole 20 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-048
AripiprazoleAripiprazole 30 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-049
AripiprazoleAripiprazole 5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3848
AripiprazoleAripiprazole 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3850
AripiprazoleAripiprazole 2 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-819
AripiprazoleAripiprazole 5 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-820
AripiprazoleAripiprazole 10 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-827
AripiprazoleAripiprazole 15 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-828
AripiprazoleAripiprazole 20 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-829
AripiprazoleAripiprazole 30 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-830
AripiprazoleAripiprazole 2 mg/1TabletOralNorthStar RxLLC16714-141
AripiprazoleAripiprazole 5 mg/1TabletOralNorthStar RxLLC16714-142
AripiprazoleAripiprazole 10 mg/1TabletOralNorthStar RxLLC16714-143
AripiprazoleAripiprazole 15 mg/1TabletOralNorthStar RxLLC16714-144
AripiprazoleAripiprazole 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3906

Showing 20 of 39.

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