NDC Package 70748-272-13 Risperidone

Injection, Powder, For Suspension, Extended Release Intramuscular - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70748-272-13
Package Description:
1 VIAL in 1 BOX / 2 mL in 1 VIAL
Product Code:
Proprietary Name:
Risperidone
Non-Proprietary Name:
Risperidone
Substance Name:
Risperidone
Usage Information:
Risperidone is used to treat certain mental/mood disorders (such as schizophrenia, bipolar disorder, irritability associated with autistic disorder). This medication can help you to think clearly and take part in everyday life. Risperidone belongs to a class of drugs called atypical antipsychotics. It works by helping to restore the balance of certain natural substances in the brain.
11-Digit NDC Billing Format:
70748027213
Product Type:
Human Prescription Drug
Labeler Name:
Lupin Pharmaceuticals, Inc.
Dosage Form:
Injection, Powder, For Suspension, Extended Release - A dried preparation intended for reconstitution to form a suspension for parenteral use which has been formulated in a manner to allow at least a reduction in dosing frequency as compared to that drug presented as a conventional dosage form (e.g., as a solution).
Administration Route(s):
Intramuscular - Administration within a muscle.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
ANDA211220
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-17-2025
End Marketing Date:
07-31-2027
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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Frequently Asked Questions

What is NDC 70748-272-13?

The NDC Packaged Code 70748-272-13 is assigned to a package of 1 vial in 1 box / 2 ml in 1 vial of Risperidone, a human prescription drug labeled by Lupin Pharmaceuticals, Inc.. The product's dosage form is injection, powder, for suspension, extended release and is administered via intramuscular form.

Is NDC 70748-272 included in the NDC Directory?

Yes, Risperidone with product code 70748-272 is active and included in the NDC Directory. The product was first marketed by Lupin Pharmaceuticals, Inc. on October 17, 2025.

What is the 11-digit format for NDC 70748-272-13?

The 11-digit format is 70748027213. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-270748-272-135-4-270748-0272-13