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  5. NDC Package Code: 72205-049-30 Aminocaproic Acid

NDC Package 72205-049-30 Aminocaproic Acid

Tablet Oral - 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:
72205-049-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
72205-049
Proprietary Name:
Aminocaproic Acid
Non-Proprietary Name:
Aminocaproic Acid
Substance Name:
Aminocaproic Acid
Usage Information:
This medication is used to help control bleeding due to a condition where your blood does not clot the way it normally should (fibrinolysis). This may cause serious bleeding after certain surgeries or in certain conditions (such as bleeding disorders, liver disease, cancer). Aminocaproic acid works by helping your blood clot normally. It belongs to a class of drugs known as antifibrinolytics.
11-Digit NDC Billing Format:
72205004930
NDC to RxNorm Crosswalk:
  • RxCUI: 197351 - aminocaproic acid 500 MG Oral Tablet
  • RxCUI: 197351 - 6-aminocaproic acid 500 MG Oral Tablet
  • RxCUI: 476271 - aminocaproic acid 1000 MG Oral Tablet
  • RxCUI: 476271 - 6-aminocaproic acid 1000 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Novadoz Pharmaceuticals Llc
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • AMINOCAPROIC ACID 500 mg/1
    • Pharmacologic Class(es):
  • Antifibrinolytic Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Fibrinolysis - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA212938
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-10-2020
    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 72205-049-30?

    The NDC Packaged Code 72205-049-30 is assigned to a package of 30 tablet in 1 bottle of Aminocaproic Acid, a human prescription drug labeled by Novadoz Pharmaceuticals Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 72205-049 included in the NDC Directory?

    Yes, Aminocaproic Acid with product code 72205-049 is active and included in the NDC Directory. The product was first marketed by Novadoz Pharmaceuticals Llc on December 10, 2020 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 72205-049-30?

    The 11-digit format is 72205004930. 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
    5-3-272205-049-305-4-272205-0049-30