NDC 53808-0162 Clonidine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0162 - Clonidine Hydrochloride
Product Characteristics
Product Packages
NDC Code 53808-0162-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0162?
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)
What is the NDC to RxNorm Crosswalk for Clonidine Hydrochloride?
- RxCUI: 884189 - cloNIDine HCl 0.3 MG Oral Tablet
- RxCUI: 884189 - clonidine hydrochloride 0.3 MG Oral Tablet
- RxCUI: 884189 - clonidine HCl 300 MCG 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".