NDC 10135-602 Felbamate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10135 - Marlex Pharmaceuticals Inc
- 10135-602 - Felbamate
Product Characteristics
ORANGE (C48331 - PEACH)
19 MM
AN;735
Product Packages
NDC Code 10135-602-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 10135-602?
What are the uses for Felbamate?
Which are Felbamate UNII Codes?
The UNII codes for the active ingredients in this product are:
- FELBAMATE (UNII: X72RBB02N8)
- FELBAMATE (UNII: X72RBB02N8) (Active Moiety)
Which are Felbamate 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Felbamate?
- RxCUI: 198358 - felbamate 400 MG Oral Tablet
- RxCUI: 198358 - FELT 400 MG Oral Tablet
- RxCUI: 198359 - felbamate 600 MG Oral Tablet
- RxCUI: 198359 - FELT 600 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Felbamate
Felbamate is used to treat certain seizures in adults and children with epilepsy whose seizures have not improved with other treatments. It is used alone or in combination with other medications to treat partial seizures in adults. It is used in combination with other medications to treat partial and generalized seizures in children with Lennox-Gastaut syndrome (a disorder that causes seizures and developmental delays). Felbamate is in a class of medications called anticonvulsants. It works by decreasing abnormal activity in the brain.
[Learn More]
* 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".