NDC codes

FDA NDC Directory
Product NDC (as listed)70518-2736Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-2736Add 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
70518-2736-0705182736007051827360030 TABLET in 1 BLISTER PACK (70518-2736-0)Marketed from May 12, 2020

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 — 2 mg/1
Dosage form
Tablet
Route
Oral
Labeler
REMEDYREPACK INC.NDC labeler code 70518
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206174
Marketing start
Listing expires
Identifiers
Product ID 70518-2736_4a8cee22-16db-98ca-e063-6294a90aa648SPL ID 4a8cee22-16db-98ca-e063-6294a90aa648SPL set ID 2bc00231-c2e7-4b9d-93a1-fb796fd8d591RxCUI 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

N470518273600 followed by a unit qualifier and the quantity

Package 70518-2736-00. 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)

AripiprazoleTabletsare indicated for the treatment of: Schizophrenia IrritabilityAssociatedwith Autistic Disorder TreatmentofTourette’s Disorder Aripiprazole is an atypical antipsychotic. Aripiprazole is 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 70518-2736

What is NDC 70518-2736?
70518-2736 is the product NDC for Aripiprazole, Aripiprazole 2 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. 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?
REMEDYREPACK INC., NDC labeler code 70518. 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 5 mg/1TabletOralBryant Ranch Prepack71335-1513
AripiprazoleAripiprazole 10 mg/1TabletOralBryant Ranch Prepack71335-1515
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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