NDC codes

FDA NDC Directory
Product NDC (as listed)69292-571Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69292-0571Add 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
69292-571-30692920571305 BLISTER PACK in 1 CARTON (69292-571-30) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Apr 1, 2026

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)
Risperidone
Generic name (nonproprietary)
risperidone
Active ingredients
Risperidone — .5 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077328
Marketing start
Listing expires
Identifiers
Product ID 69292-571_616a890a-5d6d-448b-a6d0-24759f601731SPL ID 616a890a-5d6d-448b-a6d0-24759f601731SPL set ID ca41c144-224a-4d57-88d7-8778e6c69ed2RxCUI 401953, 401954, 403825, 616698, 616705UNII L6UH7ZF8HC
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

N469292057130 followed by a unit qualifier and the quantity

Package 69292-0571-30. 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)

Risperidone orally disintegrating tablets are atypical antipsychotic indicated for: Treatment of schizophrenia ( 1.1 ) As monotherapy or adjunctive therapy with lithium or valproate, for the treatment of acute manic or mixed episodes associated with Bipolar I Disorder ( 1.2) Treatment of irritability associated with autistic disorder ( 1.3 ) 1.1 Schizophrenia Risperidone orally disintegrating tablets are indicated for the treatment of schizophrenia. Efficacy was established in 4 short-term trials in adults, 2 short-term trials in adolescents (ages 13 to 17 years), and one long-term maintenance trial in adults [see Clinical Studies (14.1) ] . 1.2 Bipolar Mania Monotherapy Risperidone orally d…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077328

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

FDA NDC Directory listings under ANDA 077328
ProductStrengthForm · routeLabelerProduct NDC
RisperidoneRisperidone 3 mg/1Tablet, Orally disintegratingOralAmici Pharma, Inc.69292-574
RisperidoneRisperidone 4 mg/1Tablet, Orally disintegratingOralAmici Pharma, Inc.69292-575
RisperidoneRisperidone 1 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-014
RisperidoneRisperidone .5 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-013
RisperidoneRisperidone 2 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-015
RisperidoneRisperidone 3 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-016
RisperidoneRisperidone 4 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-017
RisperidoneRisperidone 2 mg/1Tablet, Orally disintegratingOralAmici Pharma, Inc.69292-573
RisperidoneRisperidone 1 mg/1Tablet, Orally disintegratingOralAmici Pharma, Inc.69292-572

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