NDC 64679-720 Extended Phenytoin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64679 - Wockhardt Usa Llc.
- 64679-720 - Extended Phenytoin Sodium
Product Characteristics
Product Packages
Product Details
What is NDC 64679-720?
What are the uses for Extended Phenytoin Sodium?
Which are Extended Phenytoin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYTOIN SODIUM (UNII: 4182431BJH)
- PHENYTOIN (UNII: 6158TKW0C5) (Active Moiety)
Which are Extended Phenytoin Sodium 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:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Extended Phenytoin Sodium?
- RxCUI: 855671 - phenytoin sodium 100 MG Extended Release Oral Capsule
- RxCUI: 855671 - DPH sodium 100 MG Extended Release Oral Capsule
* Please review the disclaimer below.
Patient Education
Phenytoin
Phenytoin is used to control certain type of seizures, and to treat and prevent seizures that may begin during or after surgery to the brain or nervous system. Phenytoin is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical 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".