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  4. NDC Product Code: 52904-868 Excedrin Extra Strength

NDC 52904-868 Excedrin Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52904-868?
  5. Excedrin Extra Strength 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:
52904-868
Proprietary Name:
Excedrin Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Select Corporation
Labeler Code:
52904
Product Label ID:
60af6b21-9dc2-461e-a9bd-28d8e75cecb5
Start Marketing Date: [9]
01-23-2016
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
CAPSULE (C48336)
Size(s):
18 MM
Imprint(s):
E
Score:
1

Product Packages

NDC Code 52904-868-04

Package Description: 1 POUCH in 1 BLISTER PACK / 2 TABLET, FILM COATED in 1 POUCH

NDC Code 52904-868-05

Package Description: 2 POUCH in 1 BLISTER PACK / 2 TABLET, FILM COATED in 1 POUCH

NDC Code 52904-868-25

Package Description: 25 POUCH in 1 CARTON / 2 TABLET, FILM COATED in 1 POUCH

NDC Code 52904-868-50

Package Description: 50 POUCH in 1 CARTON / 2 TABLET, FILM COATED in 1 POUCH

Product Details

What is NDC 52904-868?

The NDC code 52904-868 is assigned by the FDA to the product Excedrin Extra Strength which is product labeled by Select Corporation. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 52904-868-04 1 pouch in 1 blister pack / 2 tablet, film coated in 1 pouch, 52904-868-05 2 pouch in 1 blister pack / 2 tablet, film coated in 1 pouch, 52904-868-25 25 pouch in 1 carton / 2 tablet, film coated in 1 pouch, 52904-868-50 50 pouch in 1 carton / 2 tablet, film coated in 1 pouch. 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 Excedrin Extra Strength?

Do not use more than directeddrink a full glass of water with each doseadults and children 12 years of age and overtake 2 caplets every 6 hours; not more than 8 caplets in 24 hoursunder 12 yearsask a doctor

Which are Excedrin Extra Strength UNII Codes?

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

Which are Excedrin Extra Strength 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 Excedrin Extra Strength?

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: 209468 - EXCEDRIN 250 MG / 250 MG / 65 MG Oral Tablet
  • RxCUI: 209468 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet [Excedrin]
  • RxCUI: 209468 - APAP 250 MG / ASA 250 MG / Caffeine 65 MG Oral Tablet [Excedrin]
  • RxCUI: 209468 - Excedrin Extra Strength (APAP 250 MG / ASA 250 MG / caffeine 65 MG) Oral Tablet
  • RxCUI: 209468 - Excedrin Menstrual Complete (APAP 250 MG / ASA 250 MG / caffeine 65 MG) 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".