NDC Package 17856-0646-2 Amantadine Hydrochloride

Solution Oral - View Billable Units, 11-Digit Format, RxNorm

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:
17856-0646-2
Package Description:
72 CUP, UNIT-DOSE in 1 PACKAGE / 5 mL in 1 CUP, UNIT-DOSE (17856-0646-4)
Product Code:
Proprietary Name:
Amantadine Hydrochloride
Non-Proprietary Name:
Amantadine Hydrochloride
Substance Name:
Amantadine Hydrochloride
Usage Information:
Amantadine hydrochloride oral solution USP is indicated for the prophylaxis and treatment of signs and symptoms of infection caused by various strains of influenza A virus. Amantadine hydrochloride is also indicated in the treatment of parkinsonism and drug-induced extrapyramidal reactions.
11-Digit NDC Billing Format:
17856064602
NDC to RxNorm Crosswalk:
  • RxCUI: 849385 - amantadine HCl 50 MG in 5 mL Oral Solution
  • RxCUI: 849385 - amantadine hydrochloride 10 MG/ML Oral Solution
  • RxCUI: 849385 - amantadine hydrochloride 50 MG per 5 ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Atlantic Biologicals Corp.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    ANDA074509
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-17-1995
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    17856-0646-172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 10 mL in 1 CUP, UNIT-DOSE (17856-0646-3)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0646-2?

    The NDC Packaged Code 17856-0646-2 is assigned to a package of 72 cup, unit-dose in 1 package / 5 ml in 1 cup, unit-dose (17856-0646-4) of Amantadine Hydrochloride, a human prescription drug labeled by Atlantic Biologicals Corp.. The product's dosage form is solution and is administered via oral form.

    Is NDC 17856-0646 included in the NDC Directory?

    Yes, Amantadine Hydrochloride with product code 17856-0646 is active and included in the NDC Directory. The product was first marketed by Atlantic Biologicals Corp. on July 17, 1995 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-0646-2?

    The 11-digit format is 17856064602. 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 5-4-1 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
    5-4-117856-0646-25-4-217856-0646-02