NDC 72022-583 Oxycodone And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72022 - Halo Pharmaceutical Inc
- 72022-583 - Oxycodone And Acetaminophen
Product Characteristics
OVAL (C48345)
14 MM
7;5;325;HL1
1
Product Packages
NDC Code 72022-583-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 72022-583-05
Package Description: 500 TABLET in 1 BOTTLE
Product Details
What is NDC 72022-583?
What are the uses for Oxycodone And Acetaminophen?
Which are Oxycodone And Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYCODONE HYDROCHLORIDE (UNII: C1ENJ2TE6C)
- OXYCODONE (UNII: CD35PMG570) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Oxycodone And Acetaminophen?
- 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
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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".