What is NDC 68788-7063?

68788-7063 is the product NDC for aripiprazole, Aripiprazole 20 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 68788-7063 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68788-7063Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68788-7063Add 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
68788-7063-1	6878870630168788706301	100 TABLET in 1 BOTTLE (68788-7063-1)Marketed from Jan 5, 2018
68788-7063-2	6878870630268788706302	20 TABLET in 1 BOTTLE (68788-7063-2)Marketed from Jan 5, 2018
68788-7063-3	6878870630368788706303	30 TABLET in 1 CARTON (68788-7063-3)Marketed from Jan 5, 2018
68788-7063-6	6878870630668788706306	60 TABLET in 1 BOTTLE (68788-7063-6)Marketed from Jan 5, 2018
68788-7063-9	6878870630968788706309	90 TABLET in 1 BOTTLE (68788-7063-9)Marketed from Jan 5, 2018

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 — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Preferred Pharmaceuticals Inc.NDC labeler code 68788
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 201519
Marketing start: Jan 5, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 68788-7063_5ef48246-f66f-4839-83df-0c0863b342ceSPL ID 5ef48246-f66f-4839-83df-0c0863b342ceSPL set ID faa3032b-d9a1-45dd-88be-abb432223f13RxCUI 349553UNII 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

N468788706301 followed by a unit qualifier and the quantity

Package 68788-7063-01. 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 3, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Aripiprazole Tablets are an atypical antipsychotic. The oral formulations are 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 ) 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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68788-7063

What is NDC 68788-7063?: 68788-7063 is the product NDC for aripiprazole, Aripiprazole 20 mg/1 tablet, listed with the FDA by Preferred Pharmaceuticals Inc.. It has 5 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?: Preferred Pharmaceuticals Inc., NDC labeler code 68788. 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 201519

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

FDA NDC Directory listings under ANDA 201519
Product	Strength	Form · route	Labeler	Product NDC
aripiprazole	Aripiprazole 5 mg/1	TabletOral	Major Pharmaceuticals	0904-6656
aripiprazole	Aripiprazole 2 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-216
aripiprazole	Aripiprazole 5 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-217
aripiprazole	Aripiprazole 10 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-218
aripiprazole	Aripiprazole 15 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-219
aripiprazole	Aripiprazole 20 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-220
aripiprazole	Aripiprazole 30 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-221
aripiprazole	Aripiprazole 5 mg/1	TabletOral	A-S Medication Solutions	50090-6563
aripiprazole	Aripiprazole 20 mg/1	TabletOral	ST. MARY'S MEDICAL PARK PHARMACY	60760-691
aripiprazole	Aripiprazole 10 mg/1	TabletOral	Bryant Ranch Prepack	63629-7003
aripiprazole	Aripiprazole 15 mg/1	TabletOral	Bryant Ranch Prepack	63629-7108
aripiprazole	Aripiprazole 2 mg/1	TabletOral	REMEDYREPACK INC.	70518-2584
aripiprazole	Aripiprazole 15 mg/1	TabletOral	REMEDYREPACK INC.	70518-2643
aripiprazole	Aripiprazole 20 mg/1	TabletOral	Bryant Ranch Prepack	71335-0412
Aripiprazole	Aripiprazole 20 mg/1	TabletOral	Direct_Rx	72189-455
aripiprazole	Aripiprazole 5 mg/1	TabletOral	Proficient Rx LP	82804-235
aripiprazole	Aripiprazole 10 mg/1	TabletOral	Proficient Rx LP	82804-236