NDC Compounded Drug 71170-950-25 Ropivacaine Hydrochloride; Fentanyl Citrate

Injection, Solution Epidural

Table of Contents

    1. Compounded Product Information
    2. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 71170-950
NDC Package Code 71170-950-25
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.		 71170095025
Package Description 250 mL in 1 BAG
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.		 Fentanyl 500mcg And Ropivacaine Hcl 250mg Added To 250ml Normal Saline
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.		 Fentanyl 500mcg 2mcg/ml And Ropivacaine Hcl 250mg Added To 250ml 0.9% Sodium Chloride Injection (for Epidural Use Only)
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.		 Ropivacaine Hydrochloride; Fentanyl Citrate
Dosage Form Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Route Name Epidural - Administration upon or over the dura mater.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 71170
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Apollo Care, Llc
Substance Name Ropivacaine Hydrochloride; Fentanyl Citrate
Active Ingredients Information 1 mg/1 mL; 2 ug/1 mL
DEA Schedule What is the Drug Enforcement Administration (DEA) CII Schedule?
The controlled substances in the CII schedule have a high abuse potential with severe psychological or physical dependence liability, but have accepted medical use in the United States. Schedule CII controlled substances include certain narcotic, stimulant, and depressant drugs. 		Schedule II (CII) Substances
Reporting Period 2021-2

Frequently Asked Questions

What is the NDC number assigned to Fentanyl 500mcg And Ropivacaine Hcl 250mg Added To 250ml Normal Saline?

Fentanyl 500mcg And Ropivacaine Hcl 250mg Added To 250ml Normal Saline was assigned by its manufacturer with NDC product code 71170-950. 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 Fentanyl 500mcg And Ropivacaine Hcl 250mg Added To 250ml Normal Saline?

The NDC package code 71170-950-25 was assigned to a 250 mL in 1 BAG of ropivacaine hydrochloride; fentanyl citrate administered epidural via injection, solution.

Who manufactures this product?

Fentanyl 500mcg And Ropivacaine Hcl 250mg Added To 250ml Normal Saline is manufactured by an outsourced facility and labeled by Apollo Care, 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.