NDC 42549-615 Oxycodone And Acetaminophen

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:
42549-615
Proprietary Name:
Oxycodone And Acetaminophen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Stat Rx Usa Llc
Labeler Code:
42549
Start Marketing Date: [9]
04-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF-WHITE)
Shape:
CAPSULE (C48336)
Size(s):
15 MM
Imprint(s):
M522;7;5;325
Score:
1

Product Packages

NDC Code 42549-615-02

Package Description: 112 TABLET in 1 BOTTLE

NDC Code 42549-615-12

Package Description: 120 TABLET in 1 BOTTLE

NDC Code 42549-615-30

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 42549-615-40

Package Description: 40 TABLET in 1 BOTTLE

NDC Code 42549-615-60

Package Description: 60 TABLET in 1 BOTTLE

NDC Code 42549-615-84

Package Description: 84 TABLET in 1 BOTTLE

NDC Code 42549-615-90

Package Description: 90 TABLET in 1 BOTTLE

Product Details

What is NDC 42549-615?

The NDC code 42549-615 is assigned by the FDA to the product Oxycodone And Acetaminophen which is product labeled by Stat Rx Usa Llc. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 42549-615-02 112 tablet in 1 bottle , 42549-615-12 120 tablet in 1 bottle , 42549-615-30 30 tablet in 1 bottle , 42549-615-40 40 tablet in 1 bottle , 42549-615-60 60 tablet in 1 bottle , 42549-615-84 84 tablet in 1 bottle , 42549-615-90 90 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: 1049225 - oxyCODONE 7.5 MG / acetaminophen 325 MG Oral Tablet
  • RxCUI: 1049225 - acetaminophen 325 MG / oxycodone hydrochloride 7.5 MG Oral Tablet
  • RxCUI: 1049225 - APAP 325 MG / oxycodone hydrochloride 7.5 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".