NDC 61919-815 Phenytoin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61919 - Direct Rx
- 61919-815 - Phenytoin Sodium
Product Characteristics
Product Packages
NDC Code 61919-815-30
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 61919-815-71
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 61919-815-72
Package Description: 120 CAPSULE in 1 BOTTLE
Product Details
What is NDC 61919-815?
What are the uses for Phenytoin Sodium?
Which are Phenytoin Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYTOIN SODIUM (UNII: 4182431BJH)
- PHENYTOIN (UNII: 6158TKW0C5) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Phenytoin Sodium?
- RxCUI: 855671 - phenytoin sodium 100 MG Extended Release Oral Capsule
- RxCUI: 855671 - DPH sodium 100 MG Extended Release Oral Capsule
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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.
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[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".