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  5. NDC Package Code: 0115-1752-08 Acitretin

NDC Package 0115-1752-08 Acitretin

Capsule 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:
0115-1752-08
Package Description:
30 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
0115-1752
Proprietary Name:
Acitretin
Non-Proprietary Name:
Acitretin
Substance Name:
Acitretin
Usage Information:
This medication is a retinoid used in the treatment of severe psoriasis and other skin disorders in adults.
11-Digit NDC Billing Format:
00115175208
NDC to RxNorm Crosswalk:
  • RxCUI: 199689 - acitretin 10 MG Oral Capsule
  • RxCUI: 199690 - acitretin 25 MG Oral Capsule
  • RxCUI: 894859 - acitretin 17.5 MG Oral Capsule
  • RxCUI: 894863 - acitretin 22.5 MG Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Amneal Pharmaceuticals Of New York Llc
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ACITRETIN 22.5 mg/1
    • Pharmacologic Class(es):
  • Retinoid - [EPC] (Established Pharmacologic Class)
  • Retinoids - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA202552
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    01-04-2016
    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 0115-1752-08?

    The NDC Packaged Code 0115-1752-08 is assigned to a package of 30 capsule in 1 bottle, plastic of Acitretin, a human prescription drug labeled by Amneal Pharmaceuticals Of New York Llc. The product's dosage form is capsule and is administered via oral form.

    Is NDC 0115-1752 included in the NDC Directory?

    Yes, Acitretin with product code 0115-1752 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Of New York Llc on January 04, 2016 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 0115-1752-08?

    The 11-digit format is 00115175208. 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
    4-4-20115-1752-085-4-200115-1752-08