ABILIFY

Product NDC
21695-003
11-digit product format
216950003
Labeler code
21695
Product ID
21695-003_217e52b5-3a7b-4bbe-af3c-b18de7d426c3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ARIPIPRAZOLE
Dosage form
TABLET
Route
ORAL
Labeler
Rebel Distributors Corp.
Application
NDA021436
Marketing category
NDA
Marketing start
2002-11-15
Marketing end
0000-00-00
Substance
ARIPIPRAZOLE
Active strength
10 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct21695-003IInactivated by FDA2026-07-31
excluded packagepackage21695-00321695-003-15IInactivated by FDA2026-07-31
excluded packagepackage21695-00321695-003-30IInactivated by FDA2026-07-31
excluded packagepackage21695-00321695-003-45IInactivated by FDA2026-07-31

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N021436-001ABILIFYARIPIPRAZOLE10MGTABLET / ORALABRLD, RS2002-11-15
N021436-002ABILIFYARIPIPRAZOLE15MGTABLET / ORALABRLD2002-11-15
N021436-003ABILIFYARIPIPRAZOLE20MGTABLET / ORALABRLD2002-11-15
N021436-004ABILIFYARIPIPRAZOLE30MGTABLET / ORALABRLD2002-11-15
N021436-005ABILIFYARIPIPRAZOLE5MGTABLET / ORALABRLD2002-11-15
N021436-006ABILIFYARIPIPRAZOLE2MGTABLET / ORALABRLD2002-11-15

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
N021436-001AB
N021436-002AB
N021436-003AB
N021436-004AB
N021436-005AB
N021436-006AB

Orange Book patents#

Application-product, Patent, Expiration table
Application-productPatentExpirationUse codeCoverage / statusSubmission date
N021436-00191259392026-07-28U-17492015-10-07
N021436-00187593502027-03-02U-15292014-07-22
N021436-00291259392026-07-28U-17492015-10-07
N021436-00287593502027-03-02U-15292014-07-22
N021436-00391259392026-07-28U-17492015-10-07
N021436-00387593502027-03-02U-15292014-07-22
N021436-00491259392026-07-28U-17492015-10-07
N021436-00487593502027-03-02U-15292014-07-22
N021436-00591259392026-07-28U-17492015-10-07
N021436-00587593502027-03-02U-15292014-07-22
N021436-00691259392026-07-28U-17492015-10-07
N021436-00687593502027-03-02U-15292014-07-22

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ABILIFYARIPIPRAZOLEOtsuka America Pharmaceutical, Inc.c040bd1d-45b7-49f2-93ea-aed7220b30ac2025-01-29Boxed warning, Warnings, Adverse reactionsExact identifier

Boxed warning cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

boxed warning

WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS and SUICIDAL THOUGHTS AND BEHAVIORS WITH ANTIDEPRESSANT DRUGS Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. ABILIFY is not approved for the treatment of patients with dementia-related psychosis [see Warnings and Precautions (5.1) ] . Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These studies did not show an increase in the risk of suicidal thoughts and behavior with antidepressant use in patients over age 24 years; there was a reduction in risk with antidepressant use in patients aged 65 years and older [see Warnings and Precautions (5.3) ] . In patients of all ages who are started on antidepressant therapy, monitor closely for worsening, and for emergence of suicidal thoughts and behaviors. Advise families and caregivers of the need for close observation and communication with the prescriber [see Warnings and Precautions (5.3) ] . WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS and SUICIDAL THOUGHTS AND BEHAVIORS WITH ANTIDEPRESSANT DRUGS See full prescribing information for complete boxed warning. Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. ABILIFY is not approved for the treatment of patients with dementia-related psychosis. ( 5.1 ) Increased risk of suicidal thinking and behavior in children, adolescents, and young adults taking antidepressants. Monitor for worsening and emergence of suicidal thoughts and behaviors. ( 5.3 )

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings and cautions

5 WARNINGS AND PRECAUTIONS Cerebrovascular Adverse Reactions in Elderly Patients with Dementia-Related Psychosis: Increased incidence of cerebrovascular adverse reactions (e.g., stroke, transient ischemic attack, including fatalities) ( 5.1 , 5.2 ) Neuroleptic Malignant Syndrome: Manage with immediate discontinuation and close monitoring ( 5.4 ) Tardive Dyskinesia: Discontinue if clinically appropriate ( 5.5 ) Metabolic Changes: Atypical antipsychotic drugs have been associated with metabolic changes that include hyperglycemia/diabetes mellitus, dyslipidemia, and body weight gain ( 5.6 ) Hyperglycemia/Diabetes Mellitus: Monitor glucose regularly in patients with and at risk for diabetes ( 5.6 ) Dyslipidemia: Undesirable alterations in lipid levels have been observed in patients treated with atypical antipsychotics ( 5.6 ) Weight Gain: Weight gain has been observed with atypical antipsychotic use. Monitor weight ( 5.6 ) Pathological Gambling and Other Compulsive Behaviors: Consider dose reduction or discontinuation ( 5.7 ) Orthostatic Hypotension: Monitor heart rate and blood pressure and warn patients with known cardiovascular or cerebrovascular disease, and risk of dehydration or syncope ( 5.8 ) Leukopenia, Neutropenia, and Agranulocytosis: have been reported with antipsychotics including ABILIFY. Patients with a history of a clinically significant low white blood cell count (WBC) or a drug-induced leukopenia/neutropenia should have their complete blood count (CBC) monitored frequently during the first few months of therapy and discontinuation of ABILIFY should be considered at the first sign of a clinically significant decline in WBC in the absence of other causative factors ( 5.10 ) Seizures/Convulsions: Use cautiously in patients with a history of seizures or with conditions that lower the seizure threshold ( 5.11 ) Potential for Cognitive and Motor Impairment: Use caution when operating machinery ( 5.12 ) Suicide: The possibility of a suicide attempt is inherent in schizophrenia and bipolar disorder. Closely supervise high-risk patients ( 5.14 ) 5.1 Increased Mortality in Elderly Patients with Dementia-Related Psychosis Increased Mortality Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. ABILIFY (aripiprazole) is not approved for the treatment of patients with dementia-related psycho...

warnings and cautions table

Table 3:Age RangeDrug-Placebo Difference in Number of Cases of Suicidality per 1000 Patients TreatedIncreases Compared to Placebo<1814 additional cases18 to 245 additional casesDecreases Compared to Placebo25 to 641 fewer case≥656 fewer cases

Adverse reactions cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

adverse reactions

6 ADVERSE REACTIONS The following adverse reactions are discussed in more detail in other sections of the labeling: Increased Mortality in Elderly Patients with Dementia-Related Psychosis [see Boxed Warning and Warnings and Precautions (5.1) ] Cerebrovascular Adverse Events, Including Stroke [see Warnings and Precautions (5.2) ] Suicidal Thoughts and Behaviors in Children, Adolescents, and Young Adults [see Boxed Warning and Warnings and Precautions (5.3) ] Neuroleptic Malignant Syndrome (NMS) [see Warnings and Precautions (5.4) ] Tardive Dyskinesia [see Warnings and Precautions (5.5) ] Metabolic Changes [see Warnings and Precautions (5.6) ] Pathological Gambling and Other Compulsive Behaviors [see Warnings and Precautions (5.7) ] Orthostatic Hypotension [see Warnings and Precautions (5.8) ] Falls [see Warnings and Precautions (5.9) ] Leukopenia, Neutropenia, and Agranulocytosis [see Warnings and Precautions (5.10) ] Seizures/Convulsions [see Warnings and Precautions (5.11) ] Potential for Cognitive and Motor Impairment [see Warnings and Precautions (5.12) ] Body Temperature Regulation [see Warnings and Precautions (5.13) ] Suicide [see Warnings and Precautions (5.14) ] Dysphagia [see Warnings and Precautions (5.15) ] Commonly observed adverse reactions (incidence ≥5% and at least twice that for placebo) were ( 6.1 ): Adult patients with schizophrenia: akathisia Pediatric patients (13 to 17 years) with schizophrenia: extrapyramidal disorder, somnolence, and tremor Adult patients (monotherapy) with bipolar mania: akathisia, sedation, restlessness, tremor, and extrapyramidal disorder Adult patients (adjunctive therapy with lithium or valproate) with bipolar mania: akathisia, insomnia, and extrapyramidal disorder Pediatric patients (10 to 17 years) with bipolar mania: somnolence, extrapyramidal disorder, fatigue, nausea, akathisia, blurred vision, salivary hypersecretion, and dizziness Adult patients with major depressive disorder (adjunctive treatment to antidepressant therapy): akathisia, restlessness, insomnia, constipation, fatigue, and blurred vision Pediatric patients (6 to 17 years) with autistic disorder: sedation, fatigue, vomiting, somnolence, tremor, pyrexia, drooling, decreased appetite, salivary hypersecretion, extrapyramidal disorder, and lethargy Pediatric patients (6 to 18 years) with Tourette's Disorder: sedation, somnolence, nausea, headach...

adverse reactions table

Table 14: Commonly Observed Adverse Reactions in Short-Term, Placebo-Controlled Trials of Adult Patients with Bipolar Mania Treated with ABILIFY MonotherapyPreferred TermPercentage of Patients Reporting ReactionABILIFY (n=917)Placebo (n=753) Akathisia134Sedation83Restlessness63Tremor63Extrapyramidal Disorder52

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
915afeb5-0b22-42c0-86ea-77abf1c5fe15Product name120250307
51c1e9bf-32c5-4a7b-b010-f93a90af7b6eProduct name120231010
34645f32-2ac4-41bf-9c61-8107e4764a26Product name120181210
f8ff9e17-cd6c-4547-98c3-f5db0d1fc25dProduct name120180110
14eaf619-f285-4cd0-9f39-d9dd8f3d9c02Product name120170824
8223ef47-de85-24dd-a9c7-5a041d2634a2Product name920170223

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21695-003-15ABILIFY15 in 1 BOTTLE, PLASTICTABLET151
21695-003-30ABILIFY30 in 1 BOTTLE, PLASTICTABLET301
21695-003-45ABILIFY45 in 1 BOTTLE, PLASTICTABLET451

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
21695-003-15EA - Each21695-003a27d0b41-a807-4f2f-9021-1285320365ea12012-07-24
21695-003-30EA - Each21695-003b03c25d1-1eeb-49ed-a4b0-7dd9ead26f5212012-07-24
21695-003-45EA - Each21695-0033018ecee-47f1-4180-89a4-59e8ed59871b12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21695-003ABILIFY (ARIPIPRAZOLE) TABLET [REBEL DISTRIBUTORS CORP.]1Legacy NDC, 3 package rows20100907_217e52b5-3a7b-4bbe-af3c-b18de7d426c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
352307ABILIFY 10 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352308ABILIFY 15 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352309ABILIFY 20 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
404602ABILIFY 5 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349545ARIPiprazole 10 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349490ARIPiprazole 15 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349553ARIPiprazole 20 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
402131ARIPiprazole 5 MG Oral TabletPSN217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352307aripiprazole 10 MG Oral Tablet [Abilify]SBD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352308aripiprazole 15 MG Oral Tablet [Abilify]SBD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352309aripiprazole 20 MG Oral Tablet [Abilify]SBD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
404602aripiprazole 5 MG Oral Tablet [Abilify]SBD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349545aripiprazole 10 MG Oral TabletSCD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349490aripiprazole 15 MG Oral TabletSCD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
349553aripiprazole 20 MG Oral TabletSCD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
402131aripiprazole 5 MG Oral TabletSCD217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352307Abilify 10 MG Oral TabletSY217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352308Abilify 15 MG Oral TabletSY217e52b5-3a7b-4bbe-af3c-b18de7d426c31
352309Abilify 20 MG Oral TabletSY217e52b5-3a7b-4bbe-af3c-b18de7d426c31
404602Abilify 5 MG Oral TabletSY217e52b5-3a7b-4bbe-af3c-b18de7d426c31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
21695-003-152169500031515 in 1 BOTTLE, PLASTICHistorical
21695-003-302169500033030 in 1 BOTTLE, PLASTICHistorical
21695-003-452169500034545 in 1 BOTTLE, PLASTICHistorical