Precedex - 0409-1660-50 - (DEXMEDETOMIDINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Precedex

Product NDC: 0409-1660
Proprietary Name: Precedex
Non Proprietary Name: DEXMEDETOMIDINE HYDROCHLORIDE
Active Ingredient(s): 4    ug/mL & nbsp;   DEXMEDETOMIDINE HYDROCHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Precedex

Product NDC: 0409-1660
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021038
Marketing Category: NDA
Start Marketing Date: 20130313

Package Information of Precedex

Package NDC: 0409-1660-50
Package Description: 20 BOTTLE in 1 TRAY (0409-1660-50) > 50 mL in 1 BOTTLE

NDC Information of Precedex

NDC Code 0409-1660-50
Proprietary Name Precedex
Package Description 20 BOTTLE in 1 TRAY (0409-1660-50) > 50 mL in 1 BOTTLE
Product NDC 0409-1660
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DEXMEDETOMIDINE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130313
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name DEXMEDETOMIDINE HYDROCHLORIDE
Strength Number 4
Strength Unit ug/mL
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC],General Anesthesia [PE]

Complete Information of Precedex


General Information