NDC 52959-539 Celebrex

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52959-539
Proprietary Name:
Celebrex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
H.j. Harkins Company, Inc.
Labeler Code:
52959
Start Marketing Date: [9]
10-02-1998
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
7767;100
7767;200
Score:
1

Product Packages

NDC Code 52959-539-00

Package Description: 100 CAPSULE in 1 BOTTLE

NDC Code 52959-539-05

Package Description: 5 CAPSULE in 1 BOTTLE

NDC Code 52959-539-07

Package Description: 7 CAPSULE in 1 BOTTLE

NDC Code 52959-539-10

Package Description: 10 CAPSULE in 1 BOTTLE

NDC Code 52959-539-14

Package Description: 14 CAPSULE in 1 BOTTLE

NDC Code 52959-539-15

Package Description: 15 CAPSULE in 1 BOTTLE

NDC Code 52959-539-20

Package Description: 20 CAPSULE in 1 BOTTLE

NDC Code 52959-539-21

Package Description: 21 CAPSULE in 1 BOTTLE

NDC Code 52959-539-28

Package Description: 28 CAPSULE in 1 BOTTLE

NDC Code 52959-539-30

Package Description: 30 CAPSULE in 1 BOTTLE

NDC Code 52959-539-40

Package Description: 40 CAPSULE in 1 BOTTLE

NDC Code 52959-539-45

Package Description: 45 CAPSULE in 1 BOTTLE

Product Details

What is NDC 52959-539?

The NDC code 52959-539 is assigned by the FDA to the product Celebrex which is product labeled by H.j. Harkins Company, Inc.. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 52959-539-00 100 capsule in 1 bottle , 52959-539-05 5 capsule in 1 bottle , 52959-539-07 7 capsule in 1 bottle , 52959-539-10 10 capsule in 1 bottle , 52959-539-14 14 capsule in 1 bottle , 52959-539-15 15 capsule in 1 bottle , 52959-539-20 20 capsule in 1 bottle , 52959-539-21 21 capsule in 1 bottle , 52959-539-28 28 capsule in 1 bottle , 52959-539-30 30 capsule in 1 bottle , 52959-539-40 40 capsule in 1 bottle , 52959-539-45 45 capsule in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Celebrex?

This medication is a nonsteroidal anti-inflammatory drug (NSAID), specifically a COX-2 inhibitor, which relieves pain and swelling (inflammation). It is used to treat arthritis, acute pain, and menstrual pain and discomfort. The pain and swelling relief provided by this medication helps you perform more of your normal daily activities. 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. This drug works by blocking the enzyme in your body that makes prostaglandins. Decreasing prostaglandins helps to reduce pain and swelling.

Which are Celebrex UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Celebrex Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Celebrex?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Celecoxib


Celecoxib is used to relieve pain, tenderness, swelling and stiffness caused by osteoarthritis (arthritis caused by a breakdown of the lining of the joints), rheumatoid arthritis (arthritis caused by swelling of the lining of the joints), and ankylosing spondylitis (arthritis that mainly affects the spine). Celecoxib is also used to treat juvenile rheumatoid arthritis (a type of arthritis that affects children) in children 2 years of age and older. Celecoxib is also used to treat painful menstrual periods and to relieve other types of short-term pain including pain caused by injuries, surgery and other medical or dental procedures, or medical conditions that last for a limited time. Celecoxib is in a class of NSAIDs called COX-2 inhibitors. It works by stopping the body's production of a substance that causes pain and inflammation.
[Learn More]


Pain Relievers


Pain relievers are medicines that reduce or relieve headaches, sore muscles, arthritis, or other aches and pains. There are many different pain medicines, and each one has advantages and risks. Some types of pain respond better to certain medicines than others. Each person may also have a slightly different response to a pain reliever.

Over-the-counter (OTC) medicines are good for many types of pain. There are two main types of OTC pain medicines: acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs (NSAIDs). Aspirin, naproxen (Aleve), and ibuprofen (Advil, Motrin) are examples of OTC NSAIDs.

If OTC medicines don't relieve your pain, your doctor may prescribe something stronger. Many NSAIDs are also available at higher prescription doses. The most powerful pain relievers are opioids. They are very effective, but they can sometimes have serious side effects. There is also a risk of addiction. Because of the risks, you must use them only under a doctor's supervision.

There are many things you can do to help ease pain. Pain relievers are just one part of a pain treatment plan.


[Learn More]


* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".