NDC 54868-5024 Oxycodone And Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5024 - Oxycodone And Acetaminophen
Product Characteristics
WHITE (C48325 - WHITE TO OFF-WHITE)
WHITE (C48325 - OFF-WHITE)
OVAL (C48345)
22 MM
15 MM
18 MM
16 MM
M562
M522;7;5;325
M582
M523;10;325
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?
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)
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:
- CROSPOVIDONE (UNII: 68401960MK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
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
* Please review the disclaimer below.
[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".