Risperidone

Product NDC
42291-912
11-digit product format
422910912
Labeler code
42291
Product ID
42291-912_48ec0cc0-9916-db6b-e063-6294a90a4bea
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Risperidone
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE
Application
ANDA078071
Marketing category
ANDA
Marketing start
2021-09-10
Substance
RISPERIDONE
Active strength
3 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

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 productproduct42291-912DDiscontinued by firm2026-07-31
excluded productproduct42291-912DDiscontinued by firm2026-07-31
excluded packagepackage42291-91242291-912-50DDiscontinued by firm2026-07-31
excluded packagepackage42291-91242291-912-60DDiscontinued by firm2026-07-31

Orange Book products#

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A078071-001RISPERIDONERISPERIDONE0.25MGTABLET / ORALAB2009-06-17
A078071-002RISPERIDONERISPERIDONE0.5MGTABLET / ORALAB2009-06-17
A078071-003RISPERIDONERISPERIDONE1MGTABLET / ORALAB2009-06-17
A078071-004RISPERIDONERISPERIDONE2MGTABLET / ORALAB2009-06-17
A078071-005RISPERIDONERISPERIDONE3MGTABLET / ORALAB2009-06-17
A078071-006RISPERIDONERISPERIDONE4MGTABLET / ORALAB2009-06-17

Therapeutic equivalence codes#

Application-product, TE code table
Application-productTE code
A078071-001AB
A078071-002AB
A078071-003AB
A078071-004AB
A078071-005AB
A078071-006AB

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
RisperidoneRISPERIDONEAmneal Pharmaceuticals NY LLCe90c886c-132a-4df6-8604-cfe5ffa49d5b2025-02-13Boxed 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 Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Risperidone is not approved for the treatment of patients with dementia-related psychosis. [see Warnings and Precautions (5.1) ] WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS 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. Risperidone is not approved for use in patients with dementia-related psychosis. ( 5.1 )

Warnings cross-check#

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

warnings and cautions

5 WARNINGS AND PRECAUTIONS Cerebrovascular events, including stroke, in elderly patients with dementia-related psychosis: Risperidone is not approved for use in patients with dementia-related psychosis. ( 5.2 ) Neuroleptic Malignant Syndrome: Manage with immediate discontinuation of risperidone and close monitoring. ( 5.3 ) Tardive dyskinesia: Consider discontinuing risperidone if clinically indicated. ( 5.4 ) Metabolic Changes: Atypical antipsychotic drugs have been associated with metabolic changes that may increase cardiovascular/ cerebrovascular risk. These metabolic changes include hyperglycemia, dyslipidemia, and weight gain. ( 5.5 ) Hyperglycemia and Diabetes Mellitus: Monitor patients for symptoms of hyperglycemia including polydipsia, polyuria, polyphagia, and weakness. Monitor glucose regularly in patients with diabetes or at risk for diabetes. ( 5.5 ) Dyslipidemia: Undesirable alterations have been observed in patients treated with atypical antipsychotics. ( 5.5 ) Weight Gain: Significant weight gain has been reported. Monitor weight gain. ( 5.5 ) Hyperprolactinemia: Prolactin elevations occur and persist during chronic administration. ( 5.6 ) Orthostatic hypotension: For patients at risk, consider a lower starting dose and slower titration. ( 5.7 ) Leukopenia, Neutropenia, and Agranulocytosis: Perform complete blood counts in patients with a history of clinically significant low white blood cell count (WBC). Consider discontinuing risperidone if a clinically significant decline in WBC occurs in the absence of other causative factors. ( 5.9 ) Potential for cognitive and motor impairment: Use caution when operating machinery. ( 5.10 ) Seizures: Use cautiously in patients with a history of seizures or with conditions that lower the seizure threshold. ( 5.11 ) 5.1 Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Analyses of 17 placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in th...

warnings and cautions table

RisperidonePlacebo1 mg/day to 8 mg/day> 8 mg/day to 16 mg/dayMean change from baseline (mg/dL)n=555n=748n=164Serum Glucose-1.40.80.6Proportion of patients with shiftsSerum Glucose0.6%0.4%0%(< 140 mg/dL to ≥ 200 mg/dL)(3/525)(3/702)(0/158)

Adverse reactions cross-check#

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

adverse reactions

6 ADVERSE REACTIONS The following 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, in elderly patients with dementia-related psychosis [see Warnings and Precautions (5.2) ] Neuroleptic malignant syndrome [see Warnings and Precautions (5.3) ] Tardive dyskinesia [see Warnings and Precautions (5.4) ] Metabolic Changes (Hyperglycemia and diabetes mellitus, Dyslipidemia, and Weight Gain) [see Warnings and Precautions (5.5) ] Hyperprolactinemia [see Warnings and Precautions (5.6) ] Orthostatic hypotension [see Warnings and Precautions (5.7) ] Falls [see Warnings and Precautions (5.8) ] Leukopenia, neutropenia, and agranulocytosis [see Warnings and Precautions (5.9) ] Potential for cognitive and motor impairment [see Warnings and Precautions (5.10) ] Seizures [see Warnings and Precautions (5.11) ] Dysphagia [see Warnings and Precautions (5.12) ] Priapism [see Warnings and Precautions (5.13) ] Disruption of body temperature regulation [see Warnings and Precautions (5.14) ] The most common adverse reactions in clinical trials (> 5% and twice placebo) were parkinsonism, akathisia, dystonia, tremor, sedation, dizziness, anxiety, blurred vision, nausea, vomiting, upper abdominal pain, stomach discomfort, dyspepsia, diarrhea, salivary hypersecretion, constipation, dry mouth, increased appetite, increased weight, fatigue, rash, nasal congestion, upper respiratory tract infection, nasopharyngitis, and pharyngolaryngeal pain. The most common adverse reactions that were associated with discontinuation from clinical trials (causing discontinuation in > 1% of adults and/or > 2% of pediatrics) were nausea, somnolence, sedation, vomiting, dizziness, and akathisia [see Adverse Reactions, Discontinuations Due to Adverse Reactions (6.1) ] . The data described in this section are derived from a clinical trial database consisting of 9803 adult and pediatric patients exposed to one or more doses of risperidone for the treatment of schizophrenia, bipolar mania, autistic disorder, and other psychiatric disorders in pediatrics and elderly patients with dementia. Of these 9803 patients, 2687 were patients who received risperidone while participating in double-blind, placebo-controlled trials. The...

adverse reactions table

Percentage of Patients Reporting ReactionRisperidoneSystem/Organ Class Adverse Reaction 2 mg per day to 8 mg per day (N=366)> 8 mg per day to 16 mg per day (N=198)Placebo (N=225)Cardiac Disorders Tachycardia 130Eye Disorders Vision blurred 311Gastrointestinal Disorders Nausea 944Constipation 896Dyspepsia 865Dry mouth 401Abdominal discomfort 311Salivary hypersecretion 21< 1Diarrhea 211General Disorders Fatigue 310Chest pain 221Asthenia 21< 1Infections and Infestations Nasopharyngitis 343Upper respiratory tract infection 231Sinusitis 121Urinary tract infection 130Investigations Blood creatine phosphokinase increased 12< 1Heart rate increased < 120Musculoskeletal and Connective Tissue DisordersBack pain 411Arthralgia 23< 1Pain in extremity 211Nervous System Disorders Parkinsonism*14178Akathisia*10103Sedation 1052Dizziness 742Dystonia*342Tremor*231Dizziness postural 200Psychiatric Disorders Insomnia 322527Anxiety 161111Respiratory, Thoracic and Mediastinal Disorders

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6ab2126a-0ca2-c16c-ab6d-b3a031ba7ac6Product name520250303
0efa9fd6-2fb6-4cd3-8b0f-2a2bf9c4a09eProduct name120250128
e457a910-2c3a-4bfd-90b9-0310982c50ddProduct name120241218
42b1a2d5-888a-4386-ab9f-0979e0d7b4aaProduct name120231010
66685e90-862d-4873-a0c5-2be73b803c36Product name120230921
92d220a1-2a4c-4393-9080-7335ca8223ccProduct name120230823

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42291-912-50Risperidone500 in 1 BOTTLETABLET5004
42291-912-60Risperidone60 in 1 BOTTLETABLET603

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-912-50EA - Each42291-912a7310c64-8ee7-46ba-afbd-444cb7da5daf12021-11-09
42291-912-60EA - Each42291-912c5fc64c3-bb4e-4a53-b44f-267c39a36fe312021-11-09

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42291-912RISPERIDONE TABLET [AVKARE]3Current NDC, Legacy NDC, 1 package rows20230111_cc97c0d4-4690-62be-e053-2a95a90a3a0c.zip
42291-912RISPERIDONE TABLET [AVKARE]2Current NDC, Legacy NDC, 1 package rows20230111_cba7628c-30b2-5d26-e053-2a95a90a3e57.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312828risperiDONE 0.25 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
312829risperiDONE 0.5 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
312830risperiDONE 1 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
312831risperiDONE 2 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
312832risperiDONE 3 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
314211risperiDONE 4 MG Oral TabletPSNcba7628c-30b2-5d26-e053-2a95a90a3e574
312828risperidone 0.25 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
312829risperidone 0.5 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
312830risperidone 1 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
312831risperidone 2 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
312832risperidone 3 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
314211risperidone 4 MG Oral TabletSCDcba7628c-30b2-5d26-e053-2a95a90a3e574
312828risperiDONE 0.25 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312829risperiDONE 0.5 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312830risperiDONE 1 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312831risperiDONE 2 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312832risperiDONE 3 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
314211risperiDONE 4 MG Oral TabletPSNcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312828risperidone 0.25 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312829risperidone 0.5 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312830risperidone 1 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312831risperidone 2 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3
312832risperidone 3 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3
314211risperidone 4 MG Oral TabletSCDcc97c0d4-4690-62be-e053-2a95a90a3a0c3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42291-912-5042291091250500 TABLET in 1 BOTTLE (42291-912-50) 500 tablet2021-09-100000-00-00NoNoCurrent
42291-912-604229109126060 TABLET in 1 BOTTLE (42291-912-60) 60 tablet2021-09-220000-00-00NoNoCurrent