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  5. NDC Package Code: 65219-184-20 Ketamine Hydrochloride

NDC Package 65219-184-20 Ketamine Hydrochloride

Injection Intramuscular; Intravenous - 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:
65219-184-20
Package Description:
10 VIAL in 1 TRAY / 20 mL in 1 VIAL (65219-184-01)
Product Code:
65219-184
Proprietary Name:
Ketamine Hydrochloride
Non-Proprietary Name:
Ketamine Hydrochloride
Substance Name:
Ketamine Hydrochloride
Usage Information:
Ketamine Hydrochloride Injection is indicated: as the sole anesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. for the induction of anesthesia prior to the administration of other general anesthetic agents. as a supplement to other anesthetic agents.
11-Digit NDC Billing Format:
65219018420
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Fresenius Kabi Usa, Llc
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
KETAMINE HYDROCHLORIDE 10 mg/mL
Pharmacologic Class(es):
DEA Schedule:
Schedule III (CIII) Substances
Sample Package:
No
FDA Application Number:
ANDA215808
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
07-10-2023
Listing Expiration Date:
12-31-2026
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 65219-184-20?

The NDC Packaged Code 65219-184-20 is assigned to a package of 10 vial in 1 tray / 20 ml in 1 vial (65219-184-01) of Ketamine Hydrochloride, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is injection and is administered via intramuscular; intravenous form.

Is NDC 65219-184 included in the NDC Directory?

Yes, Ketamine Hydrochloride with product code 65219-184 is active and included in the NDC Directory. The product was first marketed by Fresenius Kabi Usa, Llc on July 10, 2023 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 NDC billing unit for package 65219-184-20?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 65219-184-20?

The 11-digit format is 65219018420. 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
5-3-265219-184-205-4-265219-0184-20