NDC Package 0781-6021-94 Diluent

Water Solution Injection Intravenous; Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

0781-6021-94

Package Description:

1 VIAL in 1 CARTON / 50 mL in 1 VIAL

Product Code:

0781-6021

Proprietary Name:

Diluent

Non-Proprietary Name:

Water Solution

Substance Name:

Water

Usage Information:

None

11-Digit NDC Billing Format:

00781602194

Billing Unit:

ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.

NDC to RxNorm Crosswalk:

RxCUI: 349407 - treprostinil 1 MG/ML Injectable Solution

RxCUI: 349408 - treprostinil 10 MG/ML Injectable Solution

RxCUI: 349409 - treprostinil 2.5 MG/ML Injectable Solution

RxCUI: 349410 - treprostinil 5 MG/ML Injectable Solution

Product Type:

Human Prescription Drug

Labeler Name:

Sandoz 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.

Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.

Active Ingredient(s):

WATER 1 mL/mL

Sample Package:

FDA Application Number:

ANDA203649

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

03-25-2019

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

0781 - Sandoz Inc
- 0781-6021 - Diluent
  - 0781-6021-94 - 1 VIAL in 1 CARTON / 50 mL in 1 VIAL

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 0781-6021-94?

The NDC Packaged Code 0781-6021-94 is assigned to a package of 1 vial in 1 carton / 50 ml in 1 vial of Diluent, a human prescription drug labeled by Sandoz Inc. The product's dosage form is injection and is administered via intravenous; subcutaneous form.

Is NDC 0781-6021 included in the NDC Directory?

Yes, Diluent with product code 0781-6021 is active and included in the NDC Directory. The product was first marketed by Sandoz Inc on March 25, 2019 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0781-6021-94?

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 0781-6021-94?

The 11-digit format is 00781602194. 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 4-4-2 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
4-4-2	0781-6021-94	5-4-2	00781-6021-94

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