NDC Compounded Drug 69374-314-05 Midazolam

Injection, Solution Intravenous

Table of Contents

    1. Compounded Product Information
    2. NDC Crossover Products Matching Midazolam 1mg/ml
    3. Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code 69374-314
NDC Package Code 69374-314-05
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.		 69374031405
Package Description 30 CARTON in 1 CASE > 1 BOTTLE, PLASTIC in 1 CARTON > 50 mL in 1 BOTTLE, 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.		 Midazolam 1mg/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.		 Midazolam 1mg/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.		 Midazolam
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.		 This medication is used by people with epilepsy to treat a certain type of serious seizure that doesn't stop (seizure clusters). Midazolam belongs to a class of drugs known as benzodiazepines. It may work by increasing the effect of a certain substance in your body (GABA), which helps calm the brain and nerves.
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 Midazolam
Active Ingredients Information 1 mg/1 mL
DEA Schedule What is the Drug Enforcement Administration (DEA) CIV Schedule?
The controlled substances in the CIV schedule have an abuse potential and dependence liability less than those listed in CIII and have an accepted medical use in the United States. 		Schedule IV (CIV) Substances
Reporting Period 2021-2

NDC Crossover Products Matching Midazolam

NDC crossover of Midazolam 1mg/ml with NDC 69374-314 a human compounded drug with other similar products matching the same substance name (Midazolam) and the same administration route (intravenous) or dosage form (injection, solution).

Frequently Asked Questions

What is the NDC number assigned to Midazolam Hcl?

Midazolam Hcl was assigned by its manufacturer with NDC product code 69374-314. 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 Midazolam Hcl?

The NDC package code 69374-314-05 was assigned to a 30 CARTON in 1 CASE > 1 BOTTLE, PLASTIC in 1 CARTON > 50 mL in 1 BOTTLE, PLASTIC of midazolam administered intravenous via injection, solution.

Who manufactures this product?

Midazolam Hcl 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 6 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Medi-Fare Drug, Nephron Sterile Compounding Center, LLC, SterRx LLC, Apollo Care, LLC and Wells Pharma of Houston with NDC product codes 61141-1337-1, 69374-314-10, 69374-314-10, 70324-102-02, 71170-925-01 and 73702-401-02.