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  5. NDC Package Code: 0268-0141-30 Center-al - Amaranthus Retroflexus Pollen

NDC Package 0268-0141-30 Center-al - Amaranthus Retroflexus Pollen

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
0268-0141-30
Package Description:
30 mL in 1 VIAL, MULTI-DOSE
Product Code:
0268-0141
Proprietary Name:
Center-al - Amaranthus Retroflexus Pollen
Usage Information:
Hyposensitization (injection) therapy is a treatment for patients exhibiting allergic reactions to seasonal pollens, dust mites, molds, animal danders, and various other inhalants, in situations where the offending allergen cannot be avoided. Prior to the initiation of therapy, clinical sensitivity should be established by careful evaluation of the patient’s history confirmed by diagnostic skin testing. Hyposensitization should not be prescribed for sensitivities to allergens which can be easily avoided.
11-Digit NDC Billing Format:
00268014130
NDC to RxNorm Crosswalk:
  • RxCUI: 2560507 - redroot pigweed pollen extract 10000 UNT/mL Injectable Suspension
  • RxCUI: 2560507 - redroot pigweed pollen extract 10000 UNT/ML Injectable Suspension
  • RxCUI: 2560507 - Amaranthus retroflexus pollen extract 10,000 UNT/ML Injectable Suspension
  • RxCUI: 2560515 - western ragweed pollen extract 10000 UNT/mL Injectable Suspension
  • RxCUI: 2560515 - western ragweed pollen extract 10000 UNT/ML Injectable Suspension
Labeler Name:
Alk-abello, Inc.
Sample Package:
No
FDA Application Number:
BLA103753
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
01-15-1975
End Marketing Date:
05-16-2023
Listing Expiration Date:
05-16-2023
Exclude Flag:
D
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 0268-0141-30?

The NDC Packaged Code 0268-0141-30 is assigned to a package of 30 ml in 1 vial, multi-dose of Center-al - Amaranthus Retroflexus Pollen, labeled by Alk-abello, Inc.. The product's dosage form is and is administered via form.

Is NDC 0268-0141 included in the NDC Directory?

No, Center-al - Amaranthus Retroflexus Pollen with product code 0268-0141 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Alk-abello, Inc. on January 15, 1975 and its listing in the NDC Directory is set to expire on May 16, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0268-0141-30?

The 11-digit format is 00268014130. 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
4-4-20268-0141-305-4-200268-0141-30