NDC 64725-0215 Clonidine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 64725 - Tya Pharmaceuticals
- 64725-0215 - Clonidine Hydrochloride
Product Characteristics
Product Packages
NDC Code 64725-0215-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 64725-0215?
What are the uses for Clonidine Hydrochloride?
Which are Clonidine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLONIDINE HYDROCHLORIDE (UNII: W76I6XXF06)
- CLONIDINE (UNII: MN3L5RMN02) (Active Moiety)
Which are Clonidine 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Clonidine Hydrochloride?
- RxCUI: 884173 - cloNIDine HCl 0.1 MG Oral Tablet
- RxCUI: 884173 - clonidine hydrochloride 0.1 MG Oral Tablet
- RxCUI: 884173 - clonidine HCl 100 MCG 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".