NDC Compounded Drug 70092-313-50 Midazolam Hydrochloride

Injection Intravenous

Compounded Product Information
NDC Crossover Products Matching Midazolam 1mg/ml In 55ml Ns- 60ml Syr
Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code	70092-313
NDC Package Code	70092-313-50
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.	70092031350
Package Description	55 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.	Midazolam 1mg/ml In 55ml Ns- 60ml Syr
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 In 55ml Ns- 60ml Syr
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 Hydrochloride
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	70092
Labeler Name What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.	Quva Pharma, Inc.
Substance Name	Midazolam Hydrochloride
Active Ingredients Information	55 mg/55 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	2022-2

NDC Crossover Products Matching Midazolam Hydrochloride

NDC crossover of Midazolam 1mg/ml In 55ml Ns- 60ml Syr with NDC 70092-313 a human compounded drug with other similar products matching the same substance name (Midazolam Hydrochloride) and the same administration route (intravenous) or dosage form (injection).

NDC	Proprietary Name	Non-Proprietary Name	Package Desc	Dosage Form	Route Name	Company Name
70092-029-35	Midazolam 1 Mg/ml In 50ml Ns Ivb	Midazolam 1 Mg/ml In 50ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-030-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-030-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-032-50	Midazolam Pf 1mg/ml In 50ml Ns Syr	Midazolam Pf 1mg/ml In 50ml Ns Syr	50 mL in 1 SYRINGE, PLASTIC	Injection	Intravenous	Quva Pharma, Inc.
70092-032-50	Midazolam Pf 1mg/ml In 50ml Ns Syr	Midazolam Pf 1mg/ml In 50ml Ns Syr	50 mL in 1 SYRINGE, PLASTIC	Injection	Intravenous	Quva Pharma, Inc.
70092-177-35	Midazolam 1 Mg/ml In 50ml Ns Ivb	Midazolam 1 Mg/ml In 50ml Ns Ivb	50 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-177-35	Midazolam 1 Mg/ml In 50ml Ns Ivb	Midazolam 1 Mg/ml In 50ml Ns Ivb	50 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-177-35	Midazolam 1 Mg/ml In 50ml Ns Ivb	Midazolam 1 Mg/ml In 50ml Ns Ivb	50 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-177-35	Midazolam 1 Mg/ml In 50ml Ns Ivb	Midazolam 1 Mg/ml In 50ml Ns Ivb	50 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-312-75	Midazolam 1 Mg/ml 100 Ml Ns Cadd Fsff	Midazolam 1 Mg/ml 100 Ml Ns Cadd Fsff	100 mL in 1 CARTRIDGE	Injection	Intravenous	Quva Pharma, Inc.
70092-312-75	Midazolam 1 Mg/ml 100 Ml Ns Cadd Fsff	Midazolam 1 Mg/ml 100 Ml Ns Cadd Fsff	100 mL in 1 CARTRIDGE	Injection	Intravenous	Quva Pharma, Inc.
70092-418-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-418-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-418-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.
70092-418-36	Midazolam 1 Mg/ml In 100ml Ns Ivb	Midazolam 1 Mg/ml In 100ml Ns Ivb	100 mL in 1 BAG	Injection	Intravenous	Quva Pharma, Inc.

Frequently Asked Questions

What is the NDC number assigned to Midazolam 1 Mg/ml In 100ml Ns Ivb?

Midazolam 1 Mg/ml In 100ml Ns Ivb was assigned by its manufacturer with NDC product code 70092-313. 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 1 Mg/ml In 100ml Ns Ivb?

The NDC package code 70092-313-50 was assigned to a 55 mL in 1 SYRINGE of midazolam hydrochloride administered intravenous via injection.

Who manufactures this product?

Midazolam 1 Mg/ml In 100ml Ns Ivb is manufactured by an outsourced facility and labeled by Quva Pharma, Inc.. 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 15 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 70092-029-35, 70092-030-36, 70092-030-36, 70092-032-50, 70092-032-50, 70092-177-35, 70092-177-35, 70092-177-35, 70092-177-35, 70092-312-75, 70092-312-75, 70092-418-36, 70092-418-36, 70092-418-36 and 70092-418-36.

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