NDC 67296-1251 Phenytoin Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67296 - Redpharm Drug, Inc.
- 67296-1251 - Phenytoin Sodium
Product Characteristics
Product Packages
NDC Code 67296-1251-6
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 67296-1251?
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)
Which are 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:
- GELATIN (UNII: 2G86QN327L)
- LACTITOL MONOHYDRATE (UNII: UH2K6W1Y64)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- SHELLAC (UNII: 46N107B71O)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
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
* 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".