NDC 40032-431 Oxycodone Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
GRAY (C48324)
GREEN (C48329)
PINK (C48328)
BLUE (C48333)
N;25
N;21
N;27
N;23
Code Structure Chart
Product Details
What is NDC 40032-431?
What are the uses for Oxycodone Hydrochloride?
Which are Oxycodone Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYCODONE HYDROCHLORIDE (UNII: C1ENJ2TE6C)
- OXYCODONE (UNII: CD35PMG570) (Active Moiety)
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- D&C RED NO. 30 (UNII: 2S42T2808B)
What is the NDC to RxNorm Crosswalk for Oxycodone Hydrochloride?
- RxCUI: 1049611 - oxyCODONE HCl 15 MG Oral Tablet
- RxCUI: 1049611 - oxycodone hydrochloride 15 MG Oral Tablet
- RxCUI: 1049618 - oxyCODONE HCl 30 MG Oral Tablet
- RxCUI: 1049618 - oxycodone hydrochloride 30 MG Oral Tablet
- RxCUI: 1049621 - oxyCODONE HCl 5 MG Oral Tablet
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[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".