NDC Compounded Drug 73702-104-65 Dextrose Monohydrate

Injection Intravenous

Table of Contents

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

Compounded Drug Product Information

NDC Product Code 73702-104
NDC Package Code 73702-104-65
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.		 73702010465
Package Description 50 mL in 1 SYRINGE
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.		 Dextrose
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.		 Dextrose 50%
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.		 Dextrose Monohydrate
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 73702
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Wells Pharma Of Houston
Substance Name Dextrose Monohydrate
Active Ingredients Information .5 g/1 mL
Reporting Period 2023-2

NDC Crossover Products Matching Dextrose Monohydrate

NDC crossover of Dextrose with NDC 73702-104 a human compounded drug with other similar products matching the same substance name (Dextrose Monohydrate) and the same administration route (intravenous) or dosage form (injection).

Frequently Asked Questions

What is the NDC number assigned to Dextrose Pf 500mg/ml 50ml Swfi Syr?

Dextrose Pf 500mg/ml 50ml Swfi Syr was assigned by its manufacturer with NDC product code 73702-104. 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 Dextrose Pf 500mg/ml 50ml Swfi Syr?

The NDC package code 73702-104-65 was assigned to a 50 mL in 1 SYRINGE of dextrose monohydrate administered intravenous via injection.

Who manufactures this product?

Dextrose Pf 500mg/ml 50ml Swfi Syr is manufactured by an outsourced facility and labeled by Wells Pharma Of Houston. 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 1 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by QuVa Pharma, Inc. with NDC product codes 70092-475-50.