NDC codes

FDA NDC Directory
Product NDC (as listed)70748-272Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70748-0272Add 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
70748-272-13707480272131 KIT in 1 BOX (70748-272-13) * 2 mL in 1 VIAL (70748-451-11) * 2 mL in 1 SYRINGE (70748-448-01)Marketed from Oct 17, 2025

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
Dosage form
Kit
Labeler
Lupin Pharmaceuticals, Inc.NDC labeler code 70748
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211220
Marketing start
Listing expires
Identifiers
Product ID 70748-272_295a5259-e2b6-4c5c-aacb-6a85a8c4babbSPL ID 295a5259-e2b6-4c5c-aacb-6a85a8c4babbSPL set ID b462e48c-ef1d-4591-8fca-6b5829d8ed90RxCUI 402010, 402011, 402012UPC 0370748270134, 0370748272138, 0370748271131

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N470748027213 followed by a unit qualifier and the quantity

Package 70748-0272-13. 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 for extended-release injectable suspension is an atypical antipsychotic indicated: for the treatment of schizophrenia. ( 1.1 ) as monotherapy or as adjunctive therapy to lithium or valproate for the maintenance treatment of Bipolar I Disorder. ( 1.2 ) 1.1 Schizophrenia Risperidone for extended-release injectable suspension is indicated for the treatment of schizophrenia [see Clinical Studies ( 14.1 )]. 1.2 Bipolar Disorder Risperidone for extended-release injectable suspension is indicated as monotherapy or as adjunctive therapy to lithium or valproate for the maintenance treatment of Bipolar I Disorder [see Clinical Studies ( 14.2 , 14.3 )].

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70748-272

What is NDC 70748-272?
70748-272 is the product NDC for risperidone kit, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
risperidone.
Who is the labeler?
Lupin Pharmaceuticals, Inc., NDC labeler code 70748. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for risperidone?
174 other product NDCs are listed under this name. See all risperidone 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 risperidone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
RisperidoneRisperidone .5 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-01387564-0013-28
RisperidoneRisperidone 1 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-01487564-0014-28
RisperidoneRisperidone 2 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-01587564-0015-28
RisperidoneRisperidone 3 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-01687564-0016-28
RisperidoneRisperidone 4 mg/1Tablet, Orally disintegratingOralAmerisyn LLC87564-01787564-0017-28
RisperidoneRisperidone .5 mg/1TabletOralCoupler LLC67046-064467046-0644-03
RisperidoneRisperidone .25 mg/1TabletOralCoupler LLC67046-206467046-2064-03
RisperidoneRisperidone 1 mg/1TabletOralCoupler LLC67046-063567046-0635-03
RisperidoneRisperidone 2 mg/1TabletOralCoupler LLC67046-063067046-0630-03
RisperidoneRisperidone .5 mg/1Tablet, Orally disintegratingOralAmici Pharma, Inc.69292-57169292-0571-30

All 175 risperidone NDCs

Other NDCs under ANDA 211220

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

FDA NDC Directory listings under ANDA 211220
ProductStrengthForm · routeLabelerProduct NDC
risperidone—KitLupin Pharmaceuticals, Inc.70748-271
risperidone—KitLupin Pharmaceuticals, Inc.70748-270

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