Elevidys Kit
NDC 60923-535

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 60923-535?
  4. Elevidys Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

Elevidys (delandistrogene moxeparvovec-rokl) is a BLA-approved product labeled by Sarepta Therapeutics, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a kit for intravenous administration. This product entry covers the primary NDC 60923-535 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
60923-535
Proprietary Name:
Elevidys
Non-Proprietary Name: [1]
Delandistrogene Moxeparvovec-rokl
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s): [4]
Intravenous - Administration within or into a vein or veins.

Labeler & Regulatory Data

Labeler Name: [5]
Sarepta Therapeutics, Inc.
Labeler Code:
60923
Product Label ID:
3525abcd-fbd2-46c5-9706-cffdf2e8a361
HCPCS Code:
J1413 - Inj delandistrogene mox rokl
FDA Application Number: [6]
BLA125781
Marketing Category: [8]
BLA - A product marketed under an approved Biologic License Application.

Marketing Timeline

Start Marketing Date: [9]
06-22-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 60923-535?

The NDC code 60923-535 is assigned by the FDA to the product Elevidys. It is commonly known by its generic name, delandistrogene moxeparvovec-rokl. This pharmaceutical product is labeled by Sarepta Therapeutics, Inc. and is currently categorized as listed product. The medication is a kit administered via intravenous route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 60923-535-44. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

ELEVIDYS is indicated for the treatment of ambulatory pediatric patients aged 4 through 5 years with Duchenne muscular dystrophy (DMD) with a confirmed mutation in the DMD gene. This indication is approved under accelerated approval based on expression of ELEVIDYS micro-dystrophin observed in patients treated with ELEVIDYS [see Clinical Pharmacology (12), Clinical Studies (14)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

  • DELANDISTROGENE MOXEPARVOVEC (UNII: 2P6QV2ZE52)
  • DELANDISTROGENE MOXEPARVOVEC (UNII: 2P6QV2ZE52) (Active Moiety)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302)
  • ISOPROPYL ALCOHOL (UNII: ND2M416302) (Active Moiety)

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for this product?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 2641679 - delandistrogene moxeparvovec-rokl 13300000000000 VECTOR-GENOMES in 10 ML Injection
  • RxCUI: 2641679 - 10 ML delandistrogene moxeparvovec-rokl 13300000000000 VECTOR-GENOMES/ML Injection
  • RxCUI: 2641679 - delandistrogene moxeparvovec-rokl 13300000000000 VECTOR-GENOMES per 10 ML Injection
  • RxCUI: 2641685 - ELEVIDYS 13300000000000 VECTOR-GENOMES in 10 ML Injection
  • RxCUI: 2641685 - 10 ML delandistrogene moxeparvovec-rokl 13300000000000 VECTOR-GENOMES/ML Injection [Elevidys]

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What kind of product is this? Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".