NDC Package 0703-0043-01 Methylprednisolone Acetate

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory .

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:
Package Description:
Product Code:
Proprietary Name:
Methylprednisolone Acetate
Usage Information:
Methylprednisolone is used to treat pain and swelling that occurs with arthritis and other joint disorders. This medication may also be used to treat various conditions such as blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/intestinal/kidney/lung diseases, and immune system disorders. It decreases your immune system's response to these conditions and reduces symptoms such as swelling, pain, and allergic-type reactions. Talk to your doctor about the risks and benefits of methylprednisolone, especially if it is to be injected near your spine (epidural). Rare but serious side effects may occur with epidural use. Methylprednisolone is a corticosteroid hormone. Methylprednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1358610 - methylPREDNISolone acetate 40 MG/ML Injectable Suspension
  • RxCUI: 1358610 - methylprednisolone acetate 40 MG/ML Injectable Suspension
  • RxCUI: 1724880 - BUPivacaine HCl 0.5 % in 10 ML Injection
  • RxCUI: 1724880 - 10 ML bupivacaine hydrochloride 5 MG/ML Injection
  • RxCUI: 1724880 - bupivacaine HCl 0.5 % in 10 ML Injection
  • Labeler Name:
    Teva Parenteral Medicines, Inc.
    Sample Package:
    FDA Application Number:
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    End Marketing Date:
    Listing Expiration Date:
    Exclude Flag:
    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 0703-0043-01?

    The NDC Packaged Code 0703-0043-01 is assigned to a package of 1 vial, multi-dose in 1 carton / 5 ml in 1 vial, multi-dose of Methylprednisolone Acetate, labeled by Teva Parenteral Medicines, Inc.. The product's dosage form is and is administered via form.

    Is NDC 0703-0043 included in the NDC Directory?

    The product was first marketed by Teva Parenteral Medicines, Inc. on October 31, 2006 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0703-0043-01?

    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 0703-0043-01?

    The 11-digit format is 00703004301. 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 4-4-2 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