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  5. NDC Package Code: 70511-122-10 Baclofen (intrathecal)

NDC Package 70511-122-10 Baclofen (intrathecal)

Baclofen Injection Intrathecal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
70511-122-10
Package Description:
1 VIAL in 1 CARTON / 20 mL in 1 VIAL
Product Code:
70511-122
Proprietary Name:
Baclofen (intrathecal)
Non-Proprietary Name:
Baclofen
Substance Name:
Baclofen
Usage Information:
Baclofen is used to treat muscle spasms caused by certain conditions (such as multiple sclerosis, spinal cord injury/disease). It works by helping to relax the muscles.
11-Digit NDC Billing Format:
70511012210
NDC to RxNorm Crosswalk:
  • RxCUI: 1666613 - baclofen 40 MG in 20 ML (2,000 MCG/ML) Injection
  • RxCUI: 1666613 - 20 ML baclofen 2 MG/ML Injection
  • RxCUI: 1666613 - baclofen 40,000 MCG per 20 ML Injection
  • RxCUI: 308517 - baclofen 10 MG in 20 ML (500 MCG/ML) Injection
  • RxCUI: 308517 - 20 ML baclofen 0.5 MG/ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Maia Pharmaceuticals, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intrathecal - Administration within the cerebrospinal fluid at any level of the cerebrospinal axis, including injection into the cerebral ventricles.
    • Active Ingredient(s):
  • BACLOFEN 500 ug/mL
    • Pharmacologic Class(es):
  • GABA A Agonists - [MoA] (Mechanism of Action)
  • GABA B Agonists - [MoA] (Mechanism of Action)
  • gamma-Aminobutyric Acid-ergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    ANDA210048
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-25-2019
    Listing Expiration Date:
    12-31-2024
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70511-122-10?

    The NDC Packaged Code 70511-122-10 is assigned to a package of 1 vial in 1 carton / 20 ml in 1 vial of Baclofen (intrathecal), a human prescription drug labeled by Maia Pharmaceuticals, Inc.. The product's dosage form is injection and is administered via intrathecal form.

    Is NDC 70511-122 included in the NDC Directory?

    Yes, Baclofen (intrathecal) with product code 70511-122 is active and included in the NDC Directory. The product was first marketed by Maia Pharmaceuticals, Inc. on September 25, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 70511-122-10?

    The 11-digit format is 70511012210. 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
    5-3-270511-122-105-4-270511-0122-10