Tigecycline Injection, Powder, Lyophilized, For Solution
NDC Package 71288-019-92

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Tigecycline injection is tigecycline is used to treat certain serious bacterial infections when other antibiotics may not work. This formulation utilizes a injection, powder, lyophilized, for solution delivery system. Marketed by Meitheal Pharmaceuticals Inc., this product is identified by NDC 71288-019 and is authorized under FDA application ANDA214020.

Identification & Billing

NDC Package Code
71288-019-92
Package Description
10 VIAL, SINGLE-DOSE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-DOSE (71288-019-91)
Product Code
11-Digit Billing Format
71288001992
RxNorm Crosswalk
RxCUI: 581531 - tigecycline 50 MG Injection

Clinical Specifications

Proprietary Name
Tigecycline
Non-Proprietary Name
Tigecycline
Substance Name
Tigecycline
Dosage Form
Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
Administration Route
  • Intravenous - Administration within or into a vein or veins.
  • Intravenous - Administration within or into a vein or veins.
Usage Information
Tigecycline is used to treat certain serious bacterial infections when other antibiotics may not work. It is related to a class of drugs known as tetracycline antibiotics. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.

Regulatory & Marketing

Labeler Name
Meitheal Pharmaceuticals Inc.
Product Type
Human Prescription Drug
FDA Application #
ANDA214020
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
05-13-2021
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (71288-019). Click a package code to view its specific billing and regulatory data.

10 VIAL, SINGLE-DOSE in 1 CARTON / 5 mL in 1 VIAL, SINGLE-DOSE (71288-019-10)

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71288-019-92 identifies a specific commercial package of 10 vial, single-dose in 1 carton / 5 ml in 1 vial, single-dose (71288-019-91) of Tigecycline, a human prescription drug labeled by Meitheal Pharmaceuticals Inc.. This injection, powder, lyophilized, for solution is formulated for intravenous use and contains tigecycline as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Meitheal Pharmaceuticals Inc. on May 13, 2021. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Tigecycline is used to treat certain serious bacterial infections when other antibiotics may not work. It is related to a class of drugs known as tetracycline antibiotics. It works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.

How is this Meitheal Pharmaceuticals Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71288001992. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
71288-019-92
11-Digit CMS (5-4-2)
71288-0019-92

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.