NDC 54868-5684 Focalinxr
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5684 - Focalinxr
Product Characteristics
WHITE (C48325)
GREEN (C48329)
18 MM
NVR;D10
NVR;D15
NVR;D20
Product Packages
NDC Code 54868-5684-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-5684-1
Package Description: 10 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5684?
What are the uses for Focalinxr?
Which are Focalinxr UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXMETHYLPHENIDATE HYDROCHLORIDE (UNII: 1678OK0E08)
- DEXMETHYLPHENIDATE (UNII: M32RH9MFGP) (Active Moiety)
Which are Focalinxr 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:
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- GELATIN (UNII: 2G86QN327L)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- DEXTROSE (UNII: IY9XDZ35W2)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Focalinxr?
- RxCUI: 899439 - dexmethylphenidate HCl 10 MG 24HR Extended Release Oral Capsule
- RxCUI: 899439 - 24 HR dexmethylphenidate hydrochloride 10 MG Extended Release Oral Capsule
- RxCUI: 899439 - dexmethylphenidate hydrochloride 10 MG 24 HR Extended Release Oral Capsule
- RxCUI: 899441 - Focalin XR 10 MG 24HR Extended Release Oral Capsule
- RxCUI: 899441 - 24 HR dexmethylphenidate hydrochloride 10 MG Extended Release Oral Capsule [Focalin]
* 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".