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  5. NDC Package Code: 52817-815-08 Aminocaproic Acid

NDC Package 52817-815-08 Aminocaproic Acid

Solution 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:
52817-815-08
Package Description:
236.5 mL in 1 BOTTLE, PLASTIC
Product Code:
52817-815
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:
52817081508
NDC to RxNorm Crosswalk:
  • RxCUI: 582299 - aminocaproic acid 0.25 GM/mL Oral Solution
  • RxCUI: 582299 - 6-aminocaproic acid 250 MG/ML Oral Solution
  • RxCUI: 582299 - 6-aminocaproic acid 0.25 GM per ML Oral Syrup
  • RxCUI: 582299 - 6-aminocaproic acid 1.25 GM per 5 ML Oral Syrup
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Trupharma Llc
    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.
    • Active Ingredient(s):
  • AMINOCAPROIC ACID .25 g/mL
    • Pharmacologic Class(es):
  • Antifibrinolytic Agent - [EPC] (Established Pharmacologic Class)
  • Decreased Fibrinolysis - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    ANDA212494
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-25-2020
    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 52817-815-08?

    The NDC Packaged Code 52817-815-08 is assigned to a package of 236.5 ml in 1 bottle, plastic of Aminocaproic Acid, a human prescription drug labeled by Trupharma Llc. The product's dosage form is solution and is administered via oral form.

    Is NDC 52817-815 included in the NDC Directory?

    Yes, Aminocaproic Acid with product code 52817-815 is active and included in the NDC Directory. The product was first marketed by Trupharma Llc on September 25, 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 52817-815-08?

    The 11-digit format is 52817081508. 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
    5-3-252817-815-085-4-252817-0815-08