Methocarbamol Injection
NDC Package 70069-101-10

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Methocarbamol injection is methocarbamol is used to treat muscle spasms/pain. This formulation utilizes a injection delivery system. Marketed by Somerset Therapeutics, Llc, this product is identified by NDC 70069-101 and is authorized under FDA application ANDA207522.

Identification & Billing

NDC Package Code
70069-101-10
Package Description
10 VIAL in 1 CARTON / 10 mL in 1 VIAL
Product Code
70069-101
11-Digit Billing Format
70069010110
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Methocarbamol
Non-Proprietary Name
Methocarbamol
Substance Name
Methocarbamol
Dosage Form
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
METHOCARBAMOL 100 mg/mL
Pharmacologic Class
Usage Information
Methocarbamol is used to treat muscle spasms/pain. It is usually used along with rest, physical therapy, and other treatment. It works by helping to relax the muscles.

Regulatory & Marketing

Labeler Name
Somerset Therapeutics, Llc
Product Type
Human Prescription Drug
FDA Application #
ANDA207522
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
07-31-2017
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.

* 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 (70069-101). Click a package code to view its specific billing and regulatory data.

70069-101-05
5 VIAL in 1 CARTON / 10 mL in 1 VIAL
70069-101-25
25 VIAL in 1 CARTON / 10 mL in 1 VIAL

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

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 70069-101-10 identifies a specific commercial package of 10 vial in 1 carton / 10 ml in 1 vial of Methocarbamol, a human prescription drug labeled by Somerset Therapeutics, Llc. This injection is formulated for intramuscular; intravenous use and contains methocarbamol 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 July 31, 2017. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Methocarbamol is used to treat muscle spasms/pain. It is usually used along with rest, physical therapy, and other treatment. It works by helping to relax the muscles.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70069010110. 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)
70069-101-10
11-Digit CMS (5-4-2)
70069-0101-10

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