NDC 54868-6261 Methylphenidate Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6261 - Methylphenidate Hydrochloride
Product Characteristics
Product Packages
NDC Code 54868-6261-0
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-6261-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-6261?
What are the uses for Methylphenidate Hydrochloride?
Which are Methylphenidate Hydrochloride 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 Hydrochloride 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- LACTOSE (UNII: J2B2A4N98G)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SUCCINIC ACID (UNII: AB6MNQ6J6L)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Methylphenidate Hydrochloride?
- RxCUI: 1091155 - methylphenidate HCl 18 MG 24HR Extended Release Oral Tablet
- RxCUI: 1091155 - 24 HR methylphenidate hydrochloride 18 MG Extended Release Oral Tablet
- RxCUI: 1091155 - methylphenidate hydrochloride 18 MG 24 HR Extended Release Oral Tablet
- RxCUI: 1091170 - methylphenidate HCl 27 MG 24HR Extended Release Oral Tablet
- RxCUI: 1091170 - 24 HR methylphenidate hydrochloride 27 MG Extended Release Oral Tablet
* 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".