NDC Package 57582-011-01 Methylprednisolone

Powder - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
57582-011-01
Package Description:
1 kg in 1 BAG
Product Code:
Non-Proprietary Name:
Methylprednisolone
Substance Name:
Methylprednisolone
Usage Information:
Methylprednisolone is used to treat conditions such as arthritis, blood disorders, severe allergic reactions, certain cancers, eye conditions, skin/kidney/intestinal/lung diseases, and immune system disorders. It decreases your immune system's response to various diseases to reduce symptoms such as swelling, pain, and allergic-type reactions. This medication is a corticosteroid hormone. Methylprednisolone may also be used with other medications in hormone disorders.
11-Digit NDC Billing Format:
57582001101
Product Type:
Bulk Ingredient
Labeler Name:
Tianjin Tianyao Pharmaceuticals Co., Ltd.
Dosage Form:
Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
07-01-2015
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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 57582-011-01?

The NDC Packaged Code 57582-011-01 is assigned to an UNFINISHED drug package of 1 kg in 1 bag of Methylprednisolone, a bulk ingredient labeled by Tianjin Tianyao Pharmaceuticals Co., Ltd.. The product's dosage form is powder and is administered via form.

Is NDC 57582-011 included in the NDC Directory?

Yes, Methylprednisolone is an UNFINISHED PRODUCT with code 57582-011 that is active and included in the NDC Directory. The product was first marketed by Tianjin Tianyao Pharmaceuticals Co., Ltd. on July 01, 2015 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 11-digit format for NDC 57582-011-01?

The 11-digit format is 57582001101. 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
5-3-257582-011-015-4-257582-0011-01