NDC Package 73562-114-12 Zenpep

Pancrelipase Lipase,Pancrelipase Protease,Pancrelipase Amylase Capsule, Delayed Release - 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:
73562-114-12
Package Description:
12 CAPSULE, DELAYED RELEASE in 1 BOTTLE
Product Code:
Proprietary Name:
Zenpep
Non-Proprietary Name:
Pancrelipase Lipase, Pancrelipase Protease, Pancrelipase Amylase
Substance Name:
Pancrelipase Amylase; Pancrelipase Lipase; Pancrelipase Protease
Usage Information:
This medication contains digestive enzymes to help break down and digest fats, starch, and proteins in food. It is used in conditions where the pancreas cannot make or does not release enough digestive enzymes into the small intestines to digest the food (conditions such as chronic pancreatitis, cystic fibrosis, cancer of the pancreas, post-pancreatectomy, post-gastrointestinal bypass surgery).
11-Digit NDC Billing Format:
73562011412
Product Type:
Human Prescription Drug
Labeler Name:
Aimmune Therapeutics, Inc.
Dosage Form:
Capsule, Delayed Release - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin, and which releases a drug (or drugs) at a time other than promptly after administration. Enteric-coated articles are delayed release dosage forms.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    Yes
    FDA Application Number:
    BLA022210
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    11-01-2020
    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
    73562-114-01100 CAPSULE, DELAYED RELEASE in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 73562-114-12?

    The NDC Packaged Code 73562-114-12 is assigned to a package of 12 capsule, delayed release in 1 bottle of Zenpep, a human prescription drug labeled by Aimmune Therapeutics, Inc.. The product's dosage form is capsule, delayed release and is administered via oral form.

    Is NDC 73562-114 included in the NDC Directory?

    Yes, Zenpep with product code 73562-114 is active and included in the NDC Directory. The product was first marketed by Aimmune Therapeutics, Inc. on November 01, 2020 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 73562-114-12?

    The 11-digit format is 73562011412. 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
    5-3-273562-114-125-4-273562-0114-12