NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1515Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1515Add 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
71335-1515-1713351515017133515150130 TABLET in 1 BOTTLE (71335-1515-1)Marketed from Mar 16, 2020
71335-1515-2713351515027133515150260 TABLET in 1 BOTTLE (71335-1515-2)Marketed from Apr 3, 2024
71335-1515-3713351515037133515150328 TABLET in 1 BOTTLE (71335-1515-3)Marketed from Apr 3, 2024
71335-1515-4713351515047133515150490 TABLET in 1 BOTTLE (71335-1515-4)Marketed from Apr 3, 2024

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206174
Marketing start
Listing expires
Identifiers
Product ID 71335-1515_8256d2a7-8393-4b5d-a23e-bdd8c3e4e94dSPL ID 8256d2a7-8393-4b5d-a23e-bdd8c3e4e94dSPL set ID 69af5199-f872-4298-8d09-035e2127d3d4RxCUI 349545UNII 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

N471335151501 followed by a unit qualifier and the quantity

Package 71335-1515-01. 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)

Aripiprazole Oral Tablets are indicated for the treatment of: Schizophrenia Irritability Associated with Autistic Disorder Treatment of Tourette’s Disorder Aripiprazole is an atypical antipsychotic. The oral formulations are indicated for: Schizophrenia ( 14.1 ) Irritability Associated with Autistic Disorder ( 14.4 ) 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 71335-1515

What is NDC 71335-1515?
71335-1515 is the product NDC for Aripiprazole, Aripiprazole 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 4 package NDCs, 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?
Bryant Ranch Prepack, NDC labeler code 71335. 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?
254 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 255 Aripiprazole NDCs

Other NDCs under ANDA 206174

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

FDA NDC Directory listings under ANDA 206174
ProductStrengthForm · routeLabelerProduct NDC
AripiprazoleAripiprazole 2 mg/1TabletOralAjanta Pharma USA Inc.27241-051
AripiprazoleAripiprazole 5 mg/1TabletOralAjanta Pharma USA Inc.27241-052
AripiprazoleAripiprazole 10 mg/1TabletOralAjanta Pharma USA Inc.27241-053
AripiprazoleAripiprazole 15 mg/1TabletOralAjanta Pharma USA Inc.27241-054
AripiprazoleAripiprazole 20 mg/1TabletOralAjanta Pharma USA Inc.27241-055
AripiprazoleAripiprazole 30 mg/1TabletOralAjanta Pharma USA Inc.27241-056
AripiprazoleAripiprazole 10 mg/1TabletOralA-S Medication Solutions50090-6409
AripiprazoleAripiprazole 2 mg/1TabletOralCoupler LLC67046-1638
AripiprazoleAripiprazole 5 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7749
AripiprazoleAripiprazole 2 mg/1TabletOralREMEDYREPACK INC.70518-2736
AripiprazoleAripiprazole 5 mg/1TabletOralBryant Ranch Prepack71335-1513
AripiprazoleAripiprazole 2 mg/1TabletOralBryant Ranch Prepack71335-1682
AripiprazoleAripiprazole 2 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-088
AripiprazoleAripiprazole 5 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-089
AripiprazoleAripiprazole 10 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-090
AripiprazoleAripiprazole 15 mg/1TabletOralQuallent Pharmaceuticals Health LLC82009-091
AripiprazoleAripiprazole 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-006

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