NDC 54868-0733 Methylphenidate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ORANGE (C48331 - PEACH)
GREEN (C48329)
8 MM
7 MM
DAN;20;5884
DAN;10;5883
2
Code Structure Chart
Product Details
What is NDC 54868-0733?
What are the uses for Methylphenidate?
Which are Methylphenidate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYLPHENIDATE HYDROCHLORIDE (UNII: 4B3SC438HI)
- METHYLPHENIDATE (UNII: 207ZZ9QZ49) (Active Moiety)
Which are Methylphenidate 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Methylphenidate?
- RxCUI: 1091150 - methylphenidate HCl 10 MG Oral Tablet
- RxCUI: 1091150 - methylphenidate hydrochloride 10 MG Oral Tablet
- RxCUI: 1091392 - methylphenidate HCl 20 MG Oral Tablet
- RxCUI: 1091392 - methylphenidate hydrochloride 20 MG Oral Tablet
- RxCUI: 1091497 - methylphenidate HCl 5 MG Oral Tablet
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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".