NDC 63629-6834 Oxcarbazepine

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:
63629-6834
Proprietary Name:
Oxcarbazepine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
63629
Start Marketing Date: [9]
01-11-2008
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332 - BEIGE)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
B294
Score:
2

Product Packages

NDC Code 63629-6834-1

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

NDC Code 63629-6834-2

Package Description: 60 TABLET, FILM COATED in 1 BOTTLE

NDC Code 63629-6834-3

Package Description: 90 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 63629-6834?

The NDC code 63629-6834 is assigned by the FDA to the product Oxcarbazepine which is product labeled by Bryant Ranch Prepack. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 63629-6834-1 30 tablet, film coated in 1 bottle , 63629-6834-2 60 tablet, film coated in 1 bottle , 63629-6834-3 90 tablet, film coated 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 Oxcarbazepine?

Oxcarbazepine is used alone or with other medications to treat seizure disorders (epilepsy). Oxcarbazepine tablets, USP are indicated for use as monotherapy or adjunctive therapy in the treatment of partial seizures in adults and as monotherapy in the treatment of partial seizures in children aged 4 years and above with epilepsy, and as adjunctive therapy in children aged 2 years and above with partial seizures.

Which are Oxcarbazepine UNII Codes?

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

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:

What is the NDC to RxNorm Crosswalk for Oxcarbazepine?

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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Patient Education

Oxcarbazepine


Oxcarbazepine (Trileptal) is used alone or in combination with other medications to control certain types of seizures in adults and children. Oxcarbazepine extended-release tablets (Oxtellar XR) are used in combination with other medications to control certain types of seizures in adults and children 6 years of age and older. Oxcarbazepine is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.
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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".