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  5. NDC Package Code: 62135-437-30 Prednisolone

NDC Package 62135-437-30 Prednisolone

Tablet Oral - 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:
62135-437-30
Package Description:
30 TABLET in 1 BOTTLE
Product Code:
62135-437
Proprietary Name:
Prednisolone
Non-Proprietary Name:
Prednisolone
Substance Name:
Prednisolone
Usage Information:
Prednisolone is a man-made form of a natural substance (corticosteroid hormone) made by the adrenal gland. It is used to treat conditions such as arthritis, blood problems, immune system disorders, skin and eye conditions, breathing problems, cancer, and severe allergies. It decreases your immune system's response to various diseases to reduce symptoms such as pain, swelling and allergic-type reactions.
11-Digit NDC Billing Format:
62135043730
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
30 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Chartwell Rx, Llc
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
PREDNISOLONE 5 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA080531
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
05-31-1974
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 62135-437-30?

The NDC Packaged Code 62135-437-30 is assigned to a package of 30 tablet in 1 bottle of Prednisolone, a human prescription drug labeled by Chartwell Rx, Llc. The product's dosage form is tablet and is administered via oral form.

Is NDC 62135-437 included in the NDC Directory?

Yes, Prednisolone with product code 62135-437 is active and included in the NDC Directory. The product was first marketed by Chartwell Rx, Llc on May 31, 1974 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 62135-437-30?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 30.

What is the 11-digit format for NDC 62135-437-30?

The 11-digit format is 62135043730. 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
5-3-262135-437-305-4-262135-0437-30