Ropivacaine Hydrochloride Injection
NDC Package 70069-062-25

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Ropivacaine Hydrochloride injection is uSP is indicated for the production of local or regional anesthesia for surgery and for acute pain management. This formulation utilizes a injection delivery system. Marketed by Somerset Therapeutics, Llc, this product is identified by NDC 70069-062 and is authorized under FDA application ANDA207636.

Identification & Billing

NDC Package Code
70069-062-25
Package Description
25 VIAL in 1 CARTON / 20 mL in 1 VIAL (70069-062-01)
Product Code
11-Digit Billing Format
70069006225
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Ropivacaine Hydrochloride
Non-Proprietary Name
Ropivacaine Hydrochloride
Substance Name
Ropivacaine Hydrochloride
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
  • Epidural - Administration upon or over the dura mater.
  • Infiltration - Administration that results in substances passing into tissue spaces or into cells.
  • Perineural - Administration surrounding a nerve or nerves.
Active Ingredient(s)
Usage Information
Ropivacaine Hydrochloride Injection, USP is indicated for the production of local or regional anesthesia for surgery and for acute pain management. Surgical Anesthesia: epidural block for surgery including cesarean section; major nerve block; local infiltrationAcute Pain Management: epidural continuous infusion or intermittent bolus, eg, postoperative or labor; local infiltration

Regulatory & Marketing

Labeler Name
Somerset Therapeutics, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA207636
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
06-15-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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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Billing & HCPCS Mapping

To facilitate insurance claims and reimbursement, this drug package is mapped to specific HCPCS administrative codes. This crosswalk aligns clinical data with the billing standards used in ASP (Average Sales Price), AWP, and OPPS payment systems. Use the cards below to identify the correct billable units for provider claims.

Source: PDAC
INJECTION, ROPIVACAINE HYDROCHLORIDE, 1 MG
HCPCS Dosage 1 MG
Units / Pkg

Note for Medical Coders: These mappings are synthesized from various CMS datasets including OPPS, PrEP, and DAC (Data Analysis and Coding) contractors. Always confirm unit conversions against the current quarter's pricing files before final submission.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (70069-062). Click a package code to view its specific billing and regulatory data.

10 VIAL in 1 CARTON / 20 mL in 1 VIAL (70069-062-01)

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Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70069-062-25 identifies a specific commercial package of 25 vial in 1 carton / 20 ml in 1 vial (70069-062-01) of Ropivacaine Hydrochloride, a human prescription drug labeled by Somerset Therapeutics, Llc. This injection is formulated for epidural; infiltration; perineural use and contains ropivacaine hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Somerset Therapeutics, Llc on June 15, 2018. The current certification is valid through December 31, 2026.

How is this Somerset Therapeutics, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70069006225. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
70069-062-25
11-Digit CMS (5-4-2)
70069-0062-25

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.