NDC 54868-0325 Dilantin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328 - PALE PINK OPAQUE)
ORANGE (C48331 - MEDIUM ORANGE)
WHITE (C48325 - WHITE, OPAQUE)
16 MM
PD;DILANTIN;100;MG
Code Structure Chart
Product Details
What is NDC 54868-0325?
What are the uses for Dilantin?
Which are Dilantin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYTOIN SODIUM (UNII: 4182431BJH)
- PHENYTOIN (UNII: 6158TKW0C5) (Active Moiety)
Which are Dilantin 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GELATIN (UNII: 2G86QN327L)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
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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".