NDC 54868-5024 Oxycodone And Acetaminophen

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing certification is expired.
NDC Product Code:
54868-5024
Proprietary Name:
Oxycodone And Acetaminophen
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Physicians Total Care, Inc.
Labeler Code:
54868
Start Marketing Date: [9]
10-14-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
E
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
WHITE (C48325 - WHITE TO OFF-WHITE)
WHITE (C48325 - OFF-WHITE)
Shape:
ROUND (C48348)
OVAL (C48345)
Size(s):
12 MM
22 MM
15 MM
18 MM
16 MM
Imprint(s):
512
M562
M522;7;5;325
M582
M523;10;325
Score:
2
1

Product Packages

NDC Code 54868-5024-0

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 54868-5024-1

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 54868-5024-3

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 54868-5024-4

Package Description: 10 TABLET in 1 BOTTLE

NDC Code 54868-5024-5

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 54868-5024-6

Package Description: 40 TABLET in 1 BOTTLE

NDC Code 54868-5024-7

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 54868-5024-8

Package Description: 150 TABLET in 1 BOTTLE

NDC Code 54868-5024-9

Package Description: 180 TABLET in 1 BOTTLE

Product Details

What is NDC 54868-5024?

The NDC code 54868-5024 is assigned by the FDA to the product Oxycodone And Acetaminophen which is product labeled by Physicians Total Care, Inc.. The product's dosage form is . The product is distributed in 9 packages with assigned NDC codes 54868-5024-0 60 tablet in 1 bottle , 54868-5024-1 100 tablet in 1 bottle , 54868-5024-3 30 tablet in 1 bottle , 54868-5024-4 10 tablet in 1 bottle , 54868-5024-5 120 tablet in 1 bottle , 54868-5024-6 40 tablet in 1 bottle , 54868-5024-7 90 tablet in 1 bottle , 54868-5024-8 150 tablet in 1 bottle , 54868-5024-9 180 tablet 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 Oxycodone And Acetaminophen?

Oxycodone and acetaminophen tablets USP are indicated for the relief of moderate to moderately severe pain.

Which are Oxycodone And Acetaminophen UNII Codes?

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

Which are Oxycodone And Acetaminophen 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 Oxycodone And Acetaminophen?

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: 1049214 - oxyCODONE 10 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049214 - acetaminophen 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049214 - APAP 325 MG / oxycodone hydrochloride 10 MG Oral Tablet
  • RxCUI: 1049221 - oxyCODONE 5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049221 - acetaminophen 325 MG / oxycodone hydrochloride 5 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".