NDC codes

FDA NDC Directory
Product NDC (as listed)29300-179Labeler and product segments. Claims need a package NDC.
Product NDC at billing width29300-0179Add 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
29300-179-0129300017901100 TABLET in 1 BOTTLE, PLASTIC (29300-179-01)Marketed from Feb 21, 2022
29300-179-0529300017905500 TABLET in 1 BOTTLE, PLASTIC (29300-179-05)Marketed from Feb 21, 2022
29300-179-132930001791330 TABLET in 1 BOTTLE, PLASTIC (29300-179-13)Marketed from Feb 21, 2022

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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203025
Marketing start
Listing expires
Identifiers
Product ID 29300-179_f1daa6df-15e5-4f75-b656-6f99906e98e0SPL ID f1daa6df-15e5-4f75-b656-6f99906e98e0SPL set ID 349b8a7b-5ada-4f5c-a269-a86806c6b520RxCUI 349490, 349545, 349547, 349553, 402131, 602964UNII 82VFR53I78UPC 0329300180138, 0329300177138, 0329300178135, 0329300176131, 0329300179132
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

N429300017901 followed by a unit qualifier and the quantity

Package 29300-0179-01. 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 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)

Other NDCs under ANDA 203025

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

FDA NDC Directory listings under ANDA 203025
ProductStrengthForm · routeLabelerProduct NDC
AripiprazoleAripiprazole 2 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-175
AripiprazoleAripiprazole 5 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-176
AripiprazoleAripiprazole 10 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-177
AripiprazoleAripiprazole 15 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-178
AripiprazoleAripiprazole 30 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-180

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