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  5. NDC Package Code: 71335-2550-1 Diclofenac Potassium

NDC Package 71335-2550-1 Diclofenac Potassium

Capsule, Liquid Filled 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:
71335-2550-1
Package Description:
30 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code:
71335-2550
Proprietary Name:
Diclofenac Potassium
Non-Proprietary Name:
Diclofenac Potassium
Substance Name:
Diclofenac Potassium
Usage Information:
Diclofenac is used to relieve pain and swelling (inflammation) from various mild to moderate painful conditions. It is used to treat muscle aches, backaches, dental pain, menstrual cramps, and sports injuries. It also reduces pain, swelling, and joint stiffness caused by arthritis. Reducing these symptoms helps you do more of your normal daily activities. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). If you are treating a chronic condition such as arthritis, ask your doctor about non-drug treatments and/or using other medications to treat your pain. See also Warning section.
11-Digit NDC Billing Format:
71335255001
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Bryant Ranch Prepack
Dosage Form:
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DICLOFENAC POTASSIUM 25 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA022202
Marketing Category:
NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
Start Marketing Date:
03-24-2022
Listing Expiration Date:
12-31-2026
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 71335-2550-1?

The NDC Packaged Code 71335-2550-1 is assigned to a package of 30 capsule, liquid filled in 1 bottle of Diclofenac Potassium, a human prescription drug labeled by Bryant Ranch Prepack. The product's dosage form is capsule, liquid filled and is administered via oral form.

Is NDC 71335-2550 included in the NDC Directory?

Yes, Diclofenac Potassium with product code 71335-2550 is active and included in the NDC Directory. The product was first marketed by Bryant Ranch Prepack on March 24, 2022 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 71335-2550-1?

The 11-digit format is 71335255001. 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 5-4-1 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
5-4-171335-2550-15-4-271335-2550-01