NDC Compounded Drug 69374-300-05 Succinylcholine Chloride

Injection, Solution Intravenous

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Succinylcholine Chloride 20 Mg/ml
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 69374-300
NDC Package Code 69374-300-05
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.		 69374030005
Package Description 12 CARTON in 1 CASE > 30 VIAL, PLASTIC in 1 CARTON > 5 mL in 1 VIAL, PLASTIC
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.		 Succinylcholine Chloride 20 Mg/ml
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.		 Succinylcholine Chloride 20 Mg/ml
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.		 Succinylcholine Chloride
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 Intravenous - Administration within or into a vein or veins.
Marketing Category OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Code 69374
Labeler Name What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		 Nephron Sterile Compounding Center, Llc
Substance Name Succinylcholine Chloride
Active Ingredients Information 20 mg/1 mL
Reporting Period 2021-2

NDC Crossover Products Matching Succinylcholine Chloride

NDC crossover of Succinylcholine Chloride 20 Mg/ml with NDC 69374-300 a human compounded drug with other similar products matching the same substance name (Succinylcholine Chloride) and the same administration route (intravenous) or dosage form (injection, solution).

Frequently Asked Questions

What is the NDC number assigned to Succinylcholine Chloride?

Succinylcholine Chloride was assigned by its manufacturer with NDC product code 69374-300. 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 Succinylcholine Chloride?

The NDC package code 69374-300-05 was assigned to a 12 CARTON in 1 CASE > 30 VIAL, PLASTIC in 1 CARTON > 5 mL in 1 VIAL, PLASTIC of succinylcholine chloride administered intravenous via injection, solution.

Who manufactures this product?

Succinylcholine Chloride is manufactured by an outsourced facility and labeled by Nephron Sterile Compounding Center, 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 11 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Edge Pharma LLC, Medi-Fare Drug, Nephron Sterile Compounding Center, LLC, SCA Pharmaceuticals, LLC, Denver Solutions, LLC dba Leiters Health and Baycare Integrated Service Center, LLC /dba BayCare Central Pharmacy with NDC product codes 5446-1107-01, 5446-1108-01, 61141-1351-1, 69374-300-10, 69374-919-10, 69374-920-05, 70004-908-09, 70004-908-12, 71449-105-15, 71449-126-15 and 72055-001-01.