NDC 54868-5916 Vyvanse
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ORANGE (C48331 - ORANGE)
Code Structure Chart
Product Details
What is NDC 54868-5916?
What are the uses for Vyvanse?
Which are Vyvanse UNII Codes?
The UNII codes for the active ingredients in this product are:
- LISDEXAMFETAMINE DIMESYLATE (UNII: SJT761GEGS)
- LISDEXAMFETAMINE (UNII: H645GUL8KJ) (Active Moiety)
Which are Vyvanse 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Vyvanse?
- RxCUI: 854834 - lisdexamfetamine dimesylate 30 MG Oral Capsule
- RxCUI: 854836 - Vyvanse 30 MG Oral Capsule
- RxCUI: 854836 - lisdexamfetamine dimesylate 30 MG Oral Capsule [Vyvanse]
- RxCUI: 854838 - lisdexamfetamine dimesylate 40 MG Oral Capsule
- RxCUI: 854840 - Vyvanse 40 MG Oral Capsule
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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".