What is NDC 71335-1832?

71335-1832 is the product NDC for Aripiprazole, Aripiprazole 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 package NDCs, shown above in 10- and 11-digit form.

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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Aripiprazole NDC 71335-1832 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71335-1832Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71335-1832Add 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 NDC	11-digit (billing)	Package
71335-1832-1	7133518320171335183201	30 TABLET in 1 BOTTLE (71335-1832-1)Marketed from Apr 29, 2021
71335-1832-2	7133518320271335183202	28 TABLET in 1 BOTTLE (71335-1832-2)Marketed from May 3, 2022
71335-1832-3	7133518320371335183203	90 TABLET in 1 BOTTLE (71335-1832-3)Marketed from Jun 24, 2021
71335-1832-4	7133518320471335183204	60 TABLET in 1 BOTTLE (71335-1832-4)Marketed from Jun 1, 2021
71335-1832-5	7133518320571335183205	120 TABLET in 1 BOTTLE (71335-1832-5)Marketed from May 3, 2022
71335-1832-6	7133518320671335183206	15 TABLET in 1 BOTTLE (71335-1832-6)Marketed from May 3, 2022

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 — 5 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 207105
Marketing start: Feb 27, 2019
Listing expires: Dec 31, 2027
Identifiers: Product ID 71335-1832_f43ca26f-40f6-45da-a0b1-1ee42eee6962SPL ID f43ca26f-40f6-45da-a0b1-1ee42eee6962SPL set ID fb40b669-4e37-4087-8fb1-3ac140543602RxCUI 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

N471335183201 followed by a unit qualifier and the quantity

Package 71335-1832-01. 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 Jan 27, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Aripiprazole Oral Tablets, are indicated for the treatment of: Schizophrenia Acute Treatment of Manic and Mixed Episodes associated with Bipolar I Disorder Adjunctive Treatment of Major Depressive Disorder Irritability Associated with Autistic Disorder Treatment of Tourette’s Disorder Aripiprazole tablets are an atypical antipsychotic. The oral formulation is indicated for: Schizophrenia ( 14.1 ) Acute Treatment of Manic and Mixed Episodes associated with Bipolar I ( 14.2 ) Adjunctive Treatment of Major Depressive Disorder ( 14.3 ) 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 71335-1832

What is NDC 71335-1832?: 71335-1832 is the product NDC for Aripiprazole, Aripiprazole 5 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 6 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	REMEDYREPACK INC.	70518-4745	70518-4745-00
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Coupler LLC	67046-0873	67046-0873-03
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	Coupler LLC	67046-1052	67046-1052-03
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	Coupler LLC	67046-2046	67046-2046-03
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-006	87441-0006-01
Aripiprazole	Aripiprazole 20 mg/1	TabletOral	Coupler LLC	67046-1085	67046-1085-03
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	Coupler LLC	67046-0885	67046-0885-03
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	Coupler LLC	67046-1017	67046-1017-03
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Coupler LLC	67046-0492	67046-0492-03
Aripiprazole	Aripiprazole 10 mg/1	Tablet, Orally disintegratingOral	Aurobindo Pharma Limited	59651-514	59651-0514-0359651-0514-30

All 255 Aripiprazole NDCs

Other NDCs under ANDA 207105

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

FDA NDC Directory listings under ANDA 207105
Product	Strength	Form · route	Labeler	Product NDC
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3725
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	Direct_Rx	72189-466
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7733
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Direct_Rx	72189-476
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	Coupler LLC	67046-0885
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1903
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	Coupler LLC	67046-1052
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Prefferred Pharmaceuticals Inc.	68788-7808
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	Bryant Ranch Prepack	71335-1935
Aripiprazole	Aripiprazole 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-2806
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-2820
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	REMEDYREPACK INC.	70518-2869
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-2897
Aripiprazole	Aripiprazole 2 mg/1	TabletOral	Bryant Ranch Prepack	71335-1980
Aripiprazole	Aripiprazole 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-1687
Aripiprazole	Aripiprazole 10 mg/1	TabletOral	Bryant Ranch Prepack	72162-2369
Aripiprazole	Aripiprazole 30 mg/1	TabletOral	REMEDYREPACK INC.	70518-2974
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	A-S Medication Solutions	50090-4665
Aripiprazole	Aripiprazole 15 mg/1	TabletOral	Coupler LLC	67046-2046
Aripiprazole	Aripiprazole 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8089

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