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  5. NDC Package Code: 69097-008-22 Nicardipine Hydrochloride

NDC Package 69097-008-22 Nicardipine Hydrochloride

Injection 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:
69097-008-22
Package Description:
10 BAG in 1 CARTON / 200 mL in 1 BAG (69097-008-45)
Product Code:
69097-008
Proprietary Name:
Nicardipine Hydrochloride
Non-Proprietary Name:
Nicardipine Hydrochloride
Substance Name:
Nicardipine
Usage Information:
Nicardipine hydrochloride in 0.9% sodium chloride injection is indicated for the short-term treatment of hypertension when oral therapy is not feasible or desirable. For prolonged control of blood pressure, transfer patients to oral medication as soon as their clinical condition permits [see Dosage and Administration (2.6)].
11-Digit NDC Billing Format:
69097000822
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:
Cipla Usa Inc.
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
NICARDIPINE .2 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA215592
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
10-02-2024
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.

Frequently Asked Questions

What is NDC 69097-008-22?

The NDC Packaged Code 69097-008-22 is assigned to a package of 10 bag in 1 carton / 200 ml in 1 bag (69097-008-45) of Nicardipine Hydrochloride, a human prescription drug labeled by Cipla Usa Inc.. The product's dosage form is injection and is administered via intravenous form.

Is NDC 69097-008 included in the NDC Directory?

Yes, Nicardipine Hydrochloride with product code 69097-008 is active and included in the NDC Directory. The product was first marketed by Cipla Usa Inc. on October 02, 2024 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 NDC billing unit for package 69097-008-22?

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 69097-008-22?

The 11-digit format is 69097000822. 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
5-3-269097-008-225-4-269097-0008-22