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  5. NDC Package Code: 70069-753-01 Bupivacaine Hydrochloride

NDC Package 70069-753-01 Bupivacaine Hydrochloride

Injection, Solution Infiltration; Perineural - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70069-753-01
Package Description:
1 VIAL in 1 CARTON / 50 mL in 1 VIAL
Product Code:
70069-753
Proprietary Name:
Bupivacaine Hydrochloride
Non-Proprietary Name:
Bupivacaine Hydrochloride
Substance Name:
Bupivacaine Hydrochloride
Usage Information:
Bupivacaine hydrochloride injection is indicated in adults for the production of local or regional anesthesia or analgesia for surgery, dental and oral surgery procedures, diagnostic and therapeutic procedures, and for obstetrical procedures. Specific concentrations and presentations of bupivacaine hydrochloride injection are recommended for each type of block indicated to produce local or regional anesthesia or analgesia [see Dosage and Administration (2.2)].Limitations of UseNot all blocks are indicated for use with bupivacaine hydrochloride injection given clinically significant risks associated with use [see Dosage and Administration (2.2), Contraindications (4), Warnings and Precautions (5.1, 5.4, 5.5, 5.7, 5.9)].
11-Digit NDC Billing Format:
70069075301
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Somerset Therapeutics, Llc
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.
Administration Route(s):
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Perineural - Administration surrounding a nerve or nerves.
Active Ingredient(s):
BUPIVACAINE HYDROCHLORIDE 5 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA217792
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
11-27-2023
Listing Expiration Date:
12-31-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 70069-753-01 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
70069075301J0665INJECTION, BUPIVACAINE, NOT OTHERWISE SPECIFIED, 0.5 MG0.5 MG50ML

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
70069-753-1010 VIAL in 1 CARTON / 50 mL in 1 VIAL
70069-753-2525 VIAL in 1 CARTON / 50 mL in 1 VIAL

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70069-753-01?

The NDC Packaged Code 70069-753-01 is assigned to a package of 1 vial in 1 carton / 50 ml in 1 vial of Bupivacaine Hydrochloride, a human prescription drug labeled by Somerset Therapeutics, Llc. The product's dosage form is injection, solution and is administered via infiltration; perineural form.

Is NDC 70069-753 included in the NDC Directory?

Yes, Bupivacaine Hydrochloride with product code 70069-753 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics, Llc on November 27, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 70069-753-01?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 70069-753-01?

The 11-digit format is 70069075301. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-270069-753-015-4-270069-0753-01