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  4. NDC Product Code: 54868-4388 Etodolac

NDC 54868-4388 Etodolac

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 54868-4388?
  5. Etodolac 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:
54868-4388
Proprietary Name:
Etodolac
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Product Label ID:
1c49e27f-e028-4d79-b4c7-cb1c46ba8e4d
Start Marketing Date: [9]
09-13-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
GRAY (C48324)
BLUE (C48333 - LIGHT BLUE)
Shape:
OVAL (C48345)
Size(s):
18 MM
12 MM
19 MM
Imprint(s):
93;1122
93;7172
93;1118
Score:
1

Product Packages

NDC Code 54868-4388-0

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

NDC Code 54868-4388-1

Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54868-4388?

The NDC code 54868-4388 is assigned by the FDA to the product Etodolac which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 54868-4388-0 30 tablet, film coated, extended release in 1 bottle, plastic , 54868-4388-1 10 tablet, film coated, extended release 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 Etodolac?

Etodolac is used to relieve pain from various conditions. It also reduces pain, swelling, and joint stiffness from arthritis. This medication is known as a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking your body's production of certain natural substances that cause inflammation. 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.

Which are Etodolac UNII Codes?

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

Which are Etodolac 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 Etodolac?

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: 310245 - etodolac 400 MG 24HR Extended Release Oral Tablet
  • RxCUI: 310245 - 24 HR etodolac 400 MG Extended Release Oral Tablet
  • RxCUI: 310245 - etodolac 400 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 310247 - etodolac 600 MG 24HR Extended Release Oral Tablet
  • RxCUI: 310247 - 24 HR etodolac 600 MG 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".