NDC Package 73212-100-11 Dulaglutide

Powder - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
73212-100-11
Package Description:
50 g in 1 BOTTLE
Product Code:
Non-Proprietary Name:
Dulaglutide
Substance Name:
Dulaglutide
Usage Information:
Dulaglutide is used with a proper diet and exercise program to control high blood sugar in people with type 2 diabetes. Controlling high blood sugar helps prevent kidney damage, blindness, nerve problems, loss of limbs, and sexual function problems. This medication is also used to lessen the risk of a major cardiovascular event (such as heart attack or stroke) in people who already have, or are at high risk for heart/blood vessel disease. Dulaglutide is similar to a natural hormone in your body (incretin). It works by causing insulin release in response to high blood sugar (such as after a meal) and by decreasing the amount of sugar your liver makes. Dulaglutide is not a substitute for insulin if you need insulin treatment.
11-Digit NDC Billing Format:
73212010011
Product Type:
Bulk Ingredient
Labeler Name:
Qingdao Biopeptek Co., Ltd.
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
BULK INGREDIENT - A category specifying that a product is marketed as a bulk ingredient.
Start Marketing Date:
06-01-2024
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Unfinished Product:
Yes
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
73212-100-011 g in 1 BOTTLE
73212-100-055 g in 1 BOTTLE
73212-100-1010 g in 1 BOTTLE
73212-100-12100 g in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 73212-100-11?

The NDC Packaged Code 73212-100-11 is assigned to an UNFINISHED drug package of 50 g in 1 bottle of Dulaglutide, a bulk ingredient labeled by Qingdao Biopeptek Co., Ltd.. The product's dosage form is powder and is administered via form.

Is NDC 73212-100 included in the NDC Directory?

Yes, Dulaglutide is an UNFINISHED PRODUCT with code 73212-100 that is active and included in the NDC Directory. The product was first marketed by Qingdao Biopeptek Co., Ltd. on June 01, 2024 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 73212-100-11?

The 11-digit format is 73212010011. 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
5-3-273212-100-115-4-273212-0100-11