NDC 54868-2038 Phenytoin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2038 - Phenytoin
Product Characteristics
Product Packages
NDC Code 54868-2038-0
Package Description: 237 mL in 1 BOTTLE, GLASS
Product Details
What is NDC 54868-2038?
What are the uses for Phenytoin?
Which are Phenytoin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYTOIN (UNII: 6158TKW0C5)
- PHENYTOIN (UNII: 6158TKW0C5) (Active Moiety)
Which are Phenytoin 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:
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- GLYCERIN (UNII: PDC6A3C0OX)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- RAW SUGAR (UNII: 8M707QY5GH)
- POLYSORBATE 40 (UNII: STI11B5A2X)
- WATER (UNII: 059QF0KO0R)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALCOHOL (UNII: 3K9958V90M)
- VANILLIN (UNII: CHI530446X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
What is the NDC to RxNorm Crosswalk for Phenytoin?
- RxCUI: 1313112 - phenytoin 125 MG in 5 mL Oral Suspension
- RxCUI: 1313112 - phenytoin 25 MG/ML Oral Suspension
- RxCUI: 1313112 - DPH 25 MG/ML Oral Suspension
- RxCUI: 1313112 - phenytoin 100 MG per 4 ML Oral Suspension
- RxCUI: 1313112 - phenytoin 125 MG per 5 ML Oral Suspension
* 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".