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  5. NDC Package Code: 10695-164-50 Dried Aluminum Hydroxide Gel

NDC Package 10695-164-50 Dried Aluminum Hydroxide Gel

Gel - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
10695-164-50
Package Description:
5 kg in 1 CONTAINER
Product Code:
10695-164
Non-Proprietary Name:
Dried Aluminum Hydroxide Gel
Substance Name:
Aluminum Hydroxide
11-Digit NDC Billing Format:
10695016450
Product Type:
Drug For Further Processing
Labeler Name:
Willow Birch Pharma, Inc.
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Active Ingredient(s):
  • ALUMINUM HYDROXIDE 80 kg/100kg
    • Sample Package:
    N/A
    Marketing Category:
    DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
    Start Marketing Date:
    04-12-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Unfinished Product:
    Yes
    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 10695-164-50?

    The NDC Packaged Code 10695-164-50 is assigned to an UNFINISHED drug package of 5 kg in 1 container of Dried Aluminum Hydroxide Gel, drug for further processing labeled by Willow Birch Pharma, Inc.. The product's dosage form is gel and is administered via form.

    Is NDC 10695-164 included in the NDC Directory?

    Yes, Dried Aluminum Hydroxide Gel is an UNFINISHED PRODUCT with code 10695-164 that is active and included in the NDC Directory. The product was first marketed by Willow Birch Pharma, Inc. on April 12, 2023 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 10695-164-50?

    The 11-digit format is 10695016450. 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
    5-3-210695-164-505-4-210695-0164-50