NDC 40032-433 Oxycodone Hydrochloride

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:
40032-433
Proprietary Name:
Oxycodone Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Novel Laboratories, Inc.
Labeler Code:
40032
Start Marketing Date: [9]
06-12-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF-WHITE)
GRAY (C48324)
Shape:
ROUND (C48348)
Size(s):
7 MM
Imprint(s):
N;20
N;25
Score:
2

Product Packages

NDC Code 40032-433-01

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 40032-433-03

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 40032-433-05

Package Description: 500 TABLET in 1 BOTTLE

Product Details

What is NDC 40032-433?

The NDC code 40032-433 is assigned by the FDA to the product Oxycodone Hydrochloride which is product labeled by Novel Laboratories, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 40032-433-01 100 tablet in 1 bottle , 40032-433-03 30 tablet in 1 bottle , 40032-433-05 500 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 Hydrochloride?

Oxycodone hydrochloride tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate.   (1)Limitations of Use (1)Because of the risks of addiction, abuse, and misuse with opioids, even at recommended doses [see Warnings and Precautions (5.1)], reserve oxycodone hydrochloride tablets for use in patients for whom alternative treatment options (e.g., non-opioid analgesics or opioid combination products):Have not been tolerated or are not expected to be tolerated,Have not provided adequate analgesia or are not expected to provide adequate analgesia.

Which are Oxycodone Hydrochloride UNII Codes?

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

Which are Oxycodone Hydrochloride 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 Hydrochloride?

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:

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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".