1. Home
  2. Labeler Index
  3. Pharmacia & Upjohn Company Llc
  4. 0009-0900
  5. NDC Package Code: 0009-0900-20 Solu-cortef

NDC Package 0009-0900-20 Solu-cortef

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:
0009-0900-20
Package Description:
25 VIAL, SINGLE-DOSE in 1 PACKAGE / 2 mL in 1 VIAL, SINGLE-DOSE (0009-0900-13)
Product Code:
0009-0900
Proprietary Name:
Solu-cortef
Usage Information:
This medication is used to treat various conditions such as arthritis, severe allergies, blood diseases, breathing problems, certain cancers, eye diseases, intestinal disorders, and skin diseases. It weakens your immune system's response to various diseases to reduce symptoms such as swelling and allergic-type reactions. Hydrocortisone may also be used with other medications to replace certain hormones if you have decreased adrenal gland function or Addison's disease. Hydrocortisone belongs to a class of drugs known as corticosteroids. Hydrocortisone injection is used when a similar drug cannot be taken by mouth or when a very fast treatment is needed for patients with severe medical conditions. Talk to your doctor about the risks and benefits of hydrocortisone, especially if it is to be injected near your spine (epidural). Rare but serious side effects may occur with epidural use.
11-Digit NDC Billing Format:
00009090020
Labeler Name:
Pharmacia & Upjohn Company Llc
Sample Package:
No
FDA Application Number:
NDA009866
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
04-27-1980
End Marketing Date:
02-01-2015
Listing Expiration Date:
02-01-2015
Exclude Flag:
D
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
0009-0900-132 mL in 1 VIAL, SINGLE-DOSE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0009-0900-20?

The NDC Packaged Code 0009-0900-20 is assigned to a package of 25 vial, single-dose in 1 package / 2 ml in 1 vial, single-dose (0009-0900-13) of Solu-cortef, labeled by Pharmacia & Upjohn Company Llc. The product's dosage form is and is administered via form.

Is NDC 0009-0900 included in the NDC Directory?

The product was first marketed by Pharmacia & Upjohn Company Llc on April 27, 1980 and its listing in the NDC Directory is set to expire on February 01, 2015 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0009-0900-20?

The 11-digit format is 00009090020. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20009-0900-205-4-200009-0900-20