NDC 13310-119 Colcrys

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:
13310-119
Proprietary Name:
Colcrys
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ar Scientific Inc.
Labeler Code:
13310
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - FILM COATED)
Shape:
OVAL (C48345)
Size(s):
8 MM
Imprint(s):
AR;374
Score:
2

Product Packages

NDC Code 13310-119-01

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Price per Unit: $5.27499 per EA

NDC Code 13310-119-03

Package Description: 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Code 13310-119-05

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Code 13310-119-06

Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Code 13310-119-07

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Price per Unit: $5.27499 per EA

NDC Code 13310-119-10

Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Product Details

What is NDC 13310-119?

The NDC code 13310-119 is assigned by the FDA to the product Colcrys which is product labeled by Ar Scientific Inc.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 13310-119-01 100 tablet, film coated in 1 bottle, plastic , 13310-119-03 250 tablet, film coated in 1 bottle, plastic , 13310-119-05 500 tablet, film coated in 1 bottle, plastic , 13310-119-06 60 tablet, film coated in 1 bottle, plastic , 13310-119-07 30 tablet, film coated in 1 bottle, plastic , 13310-119-10 1000 tablet, film coated in 1 bottle, plastic . 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 Colcrys?

This medication is used to prevent or treat gout attacks (flares). Usually gout symptoms develop suddenly and involve only one or a few joints. The big toe, knee, or ankle joints are most often affected. Gout is caused by too much uric acid in the blood. When uric acid levels in the blood are too high, the uric acid may form hard crystals in your joints. Colchicine works by decreasing swelling and lessening the build up of uric acid crystals that cause pain in the affected joint(s). This medication is also used to prevent attacks of pain in the abdomen, chest, or joints caused by a certain inherited disease (familial Mediterranean fever). It is thought to work by decreasing your body's production of a certain protein (amyloid A) that builds up in people with familial Mediterranean fever. Colchicine is not a pain medication and should not be used to relieve other causes of pain.

Which are Colcrys UNII Codes?

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

Which are Colcrys 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 Colcrys?

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.

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".