NDC Compounded Drug 70092-443-43 Lidocaine Hydrochloride

Solution Intravenous

Compounded Product Information
NDC Crossover Products Matching Lido 1% Bicarb Pf 1 Ml-3 Ml Syr
Frequently Asked Questions

Compounded Drug Product Information

NDC Product Code	70092-443
NDC Package Code	70092-443-43
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.	70092044343
Package Description	1 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.	Lido 1% Bicarb Pf 1 Ml-3 Ml 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.	Lido 1% Bicarb Pf 1 Ml-3 Ml 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.	Lidocaine Hydrochloride
Dosage Form	Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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	Lidocaine Hydrochloride
Active Ingredients Information	9.1 mg/1 mL
Reporting Period	2025-1

NDC Crossover Products Matching Lidocaine Hydrochloride

NDC crossover of Lido 1% Bicarb Pf 1 Ml-3 Ml Syr with NDC 70092-443 a human compounded drug with other similar products matching the same substance name (Lidocaine Hydrochloride) and the same administration route (intravenous) or dosage form (solution).

NDC	Proprietary Name	Non-Proprietary Name	Package Desc	Dosage Form	Route Name	Company Name
69194-740-01	740 Lidocaine Hcl 4% Bottle	Lidocaine Hcl	3 mL in 1 BOTTLE, DROPPER	Solution	Ophthalmic	Pine Pharmaceuticals Llc
69194-740-01	740 Lidocaine Hcl 4% Bottle	Lidocaine Hcl	3 mL in 1 BOTTLE, DROPPER	Solution	Ophthalmic	Pine Pharmaceuticals Llc
70092-175-46	Lidocaine 1% Bicarb 10 Ml Syr Pf	Lidocaine 1% Bicarb 10 Ml Syr Pf	10 mL in 1 SYRINGE	Solution	Infiltration	Quva Pharma, Inc.
70092-175-46	Lidocaine 1% Bicarb 10 Ml Syr Pf	Lidocaine 1% Bicarb 10 Ml Syr Pf	10 mL in 1 SYRINGE	Solution	Infiltration	Quva Pharma, Inc.
71286-6006-1	Lidocaine 2%	Lidocaine 2%	5 mL in 1 SYRINGE	Solution	Intravenous	Central Admixture Pharmacy Services, Inc.
72196-6006-1	Lidocaine 2%	Lidocaine 2%	5 mL in 1 SYRINGE	Solution	Intravenous	Central Admixture Pharmacy Services, Inc.

Frequently Asked Questions

What is the NDC number assigned to Lidocaine 2%?

Lidocaine 2% was assigned by its manufacturer with NDC product code 70092-443. 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 Lidocaine 2%?

The NDC package code 70092-443-43 was assigned to a 1 mL in 1 SYRINGE of lidocaine hydrochloride administered intravenous via solution.

Who manufactures this product?

Lidocaine 2% 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 6 matching products that have the same substance, dosage form and administration route. The matching products are manufactured by Pine Pharmaceuticals LLC, QuVa Pharma, Inc. and Central Admixture Pharmacy Services, Inc. with NDC product codes 69194-740-01, 69194-740-01, 70092-175-46, 70092-175-46, 71286-6006-1 and 72196-6006-1.

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