NDC 54868-6129 Oxcarbazepine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6129 - Oxcarbazepine
Product Characteristics
15 MM
19 MM
G;4
G;13;9
Product Packages
NDC Code 54868-6129-0
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-6129-1
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-6129-2
Package Description: 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-6129?
What are the uses for Oxcarbazepine?
Which are Oxcarbazepine UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXCARBAZEPINE (UNII: VZI5B1W380)
- OXCARBAZEPINE (UNII: VZI5B1W380) (Active Moiety)
Which are Oxcarbazepine 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MEGLUMINE (UNII: 6HG8UB2MUY)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Oxcarbazepine?
- RxCUI: 312136 - OXcarbazepine 150 MG Oral Tablet
- RxCUI: 312136 - oxcarbazepine 150 MG Oral Tablet
- RxCUI: 312137 - OXcarbazepine 300 MG Oral Tablet
- RxCUI: 312137 - oxcarbazepine 300 MG Oral Tablet
- RxCUI: 312138 - OXcarbazepine 600 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".