NDC Compounded Drug 69389-062-29

Injection Intravenous; Parenteral

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Ethanol Diluant
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 69389-062
NDC Package Code 69389-062-29
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.		 69389006229
Package Description 65 mL in 1 VIAL, SINGLE-USE
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.		 Ethanol Diluant
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.		 95% Ethanol
Dosage Form Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Route Name Intravenous; Parenteral -
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 69389
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Us Specialty Formulations Llc
Reporting Period 2023-1

NDC Crossover Products Matching

NDC crossover of Ethanol Diluant with NDC 69389-062 a human compounded drug with other similar products matching the same substance name () and the same administration route (intravenous; parenteral) or dosage form (injection).

Frequently Asked Questions

What is the NDC number assigned to Nandrolone Decanoate 200mg/ml?

Nandrolone Decanoate 200mg/ml was assigned by its manufacturer with NDC product code 69389-062. 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 Nandrolone Decanoate 200mg/ml?

The NDC package code 69389-062-29 was assigned to a 65 mL in 1 VIAL, SINGLE-USE of administered intravenous; parenteral via injection.

Who manufactures this product?

Nandrolone Decanoate 200mg/ml is manufactured by an outsourced facility and labeled by Us Specialty Formulations Llc. 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 30 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Hybrid Pharma with NDC product codes 26436-0649-3, 26436-0649-3, 26436-0649-3, 26436-1963-3, 26436-1963-3, 26436-2632-3, 26436-2632-3, 26436-3169-3, 26436-5000-1, 26436-5000-1, 26436-5001-5, 26436-5001-5, 26436-5001-5, 26436-5005-2, 26436-5005-2, 26436-5005-2, 26436-5007-3, 26436-5007-3, 26436-5007-3, 26436-5009-3, 26436-5009-3, 26436-5009-3, 26436-5015-3, 26436-5015-3, 26436-5015-3, 26436-5021-3, 26436-5021-3, 26436-5021-3, 26436-5022-1 and 26436-5022-1.