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  4. NDC Product Code: 21695-040 Diclofenac Sodium Extended-release

NDC 21695-040 Diclofenac Sodium Extended-release

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 21695-040?
  5. Diclofenac Sodium Extended-release Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
21695-040
Proprietary Name:
Diclofenac Sodium Extended-release
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rebel Distributors Corp.
Labeler Code:
21695
Product Label ID:
688fa1d0-6e17-4191-8618-8f62bc7765d3
Start Marketing Date: [9]
01-07-2002
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
717
Score:
1

Code Structure Chart

Product Details

What is NDC 21695-040?

The NDC code 21695-040 is assigned by the FDA to the product Diclofenac Sodium Extended-release which is product labeled by Rebel Distributors Corp.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 21695-040-30 30 tablet, extended release in 1 bottle , 21695-040-60 60 tablet, extended release in 1 bottle , 21695-040-90 90 tablet, extended release 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 Diclofenac Sodium Extended-release?

Carefully consider the potential benefits and risks of diclofenac sodium extended-release and other treatment options before deciding to use diclofenac sodium extended-release. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS).Diclofenac sodium extended-release tablets are indicated:• For relief of signs and symptoms of osteoarthritis• For relief of signs and symptoms of rheumatoid arthritis

Which are Diclofenac Sodium Extended-release UNII Codes?

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

Which are Diclofenac Sodium Extended-release 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 Diclofenac Sodium Extended-release?

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:
  • RxCUI: 855657 - diclofenac sodium 100 MG 24HR Extended Release Oral Tablet
  • RxCUI: 855657 - 24 HR diclofenac sodium 100 MG Extended Release Oral Tablet
  • RxCUI: 855657 - diclofenac sodium 100 MG 24 HR Extended Release Oral Tablet

* 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".