NDC Compounded Drug 72682-3315-1 Edetate Disodium

Injection Intravenous

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Edetate Disodium (pf) 150mg/ml 10ml
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 72682-3315
NDC Package Code 72682-3315-1
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.		 72682331501
Package Description 10 mL in 1 VIAL
Product Type 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.		 Human Compounded Drug
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.		 Edetate Disodium (pf) 150mg/ml 10ml
Non-Proprietary Name 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.		 Edetate Disodium (pf) 150mg/ml 10ml
Substance Name What is the Substance Name?
An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.		 Edetate Disodium
Dosage Form Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Route Name Intravenous - Administration within or into a vein or veins.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 72682
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Anazaohealth Corporation
Substance Name Edetate Disodium
Active Ingredients Information 150 mg/1 mL
Reporting Period 2022-2

NDC Crossover Products Matching Edetate Disodium

NDC crossover of Edetate Disodium (pf) 150mg/ml 10ml with NDC 72682-3315 a human compounded drug with other similar products matching the same substance name (Edetate Disodium) and the same administration route (intravenous) or dosage form (injection).

Frequently Asked Questions

What is the NDC number assigned to Edetate Disodium?

Edetate Disodium was assigned by its manufacturer with NDC product code 72682-3315. This product is a drug classified as a human compounded drug. Compounded drugs are medications created by combining or altering existing drugs to meet the specific needs of certain patients. The NDC directory only includes information about compounded drugs from facilities that choose to assign NDC numbers to their products.

Which are the NDC package codes for Edetate Disodium?

The NDC package code 72682-3315-1 was assigned to a 10 mL in 1 VIAL of edetate disodium administered intravenous via injection.

Who manufactures this product?

Edetate Disodium is manufactured by an outsourced facility and labeled by Anazaohealth Corporation. All compounded drugs included in the NDC directory are classified as "Outsourcing Facility Compounded Human Drug Product (Exempt from Approval Requirements)". Outsourcing facilities are a type of drug compounding facility regulated under Section 503B of the FD&C Act could be eligible for exemptions from drug registration if they meet all the conditions specified under Section 503B.

Which are the NDC crossover matchings for this product?

We found 3 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Hybrid Pharma and Empower Pharmacy with NDC product codes 26436-5023-5, 26436-5023-5 and 72627-2401-1.