NDC codes

FDA NDC Directory
Product NDC (as listed)50268-088Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50268-0088Add 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
50268-088-155026800881550 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-088-15) / 1 TABLET in 1 BLISTER PACK (50268-088-11)Marketed from Apr 28, 2016

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
AvPAKNDC labeler code 50268
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 205064
Marketing start
Listing expires
Identifiers
Product ID 50268-088_3d49db38-3629-6bb9-e063-6294a90a4b4aSPL ID 3d49db38-3629-6bb9-e063-6294a90a4b4aSPL set ID 7df4c83e-13d8-25b1-57eb-08d26ba03565RxCUI 349490, 349545, 349547, 349553, 402131, 602964UNII 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

N450268008815 followed by a unit qualifier and the quantity

Package 50268-0088-15. 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 • Treatment of Tourette’s Disorder Aripiprazole tablets are an atypical antipsychotic. The oral formulations are indicated for: • Schizophrenia (14.1) • Treatment of Tourette’s disorder (14.5)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50268-088

What is NDC 50268-088?
50268-088 is the product NDC for Aripiprazole, Aripiprazole 5 mg/1 tablet, listed with the FDA by AvPAK. 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?
AvPAK, NDC labeler code 50268. 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 2 mg/1TabletOralCoupler LLC67046-105267046-1052-03
AripiprazoleAripiprazole 15 mg/1TabletOralCoupler LLC67046-204667046-2046-03
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 30 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-158
AripiprazoleAripiprazole 15 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-156
AripiprazoleAripiprazole 20 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-157
AripiprazoleAripiprazole 15 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-183
AripiprazoleAripiprazole 2 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-180
AripiprazoleAripiprazole 5 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-181
AripiprazoleAripiprazole 10 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-182
AripiprazoleAripiprazole 20 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-184
AripiprazoleAripiprazole 30 mg/1TabletOralXLCare Pharmaceuticals, Inc.72865-185
AripiprazoleAripiprazole 10 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-046
AripiprazoleAripiprazole 2 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-044
AripiprazoleAripiprazole 5 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-045
AripiprazoleAripiprazole 30 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-049
AripiprazoleAripiprazole 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-462
AripiprazoleAripiprazole 15 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-047
AripiprazoleAripiprazole 20 mg/1TabletOralExelan Pharmaceuticals, Inc.76282-048
AripiprazoleAripiprazole 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3850
AripiprazoleAripiprazole 5 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3848
AripiprazoleAripiprazole 2 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-819
AripiprazoleAripiprazole 5 mg/1TabletOralCamber Pharmaceuticals, Inc.31722-820

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Aripiprazole NDC 50268-088 | National Drug Code | Med-Code