MIDAZOLAM HCL - midazolam hydrochloride injection, solution 
Cantrell Drug Company

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Midazolam HCl 1 mg/mL in 0.9% Sodium Chloride 2 mL Syringe

Label

image description

MIDAZOLAM HCL 
midazolam hcl injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-001
Route of Administration INTRAVENOUS DEA Schedule CIV    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MIDAZOLAM HYDROCHLORIDE (UNII: W7TTW573JJ) (MIDAZOLAM - UNII:R60L0SM5BC) MIDAZOLAM 1 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
EDETATE DISODIUM (UNII: 7FLD91C86K) 0.02 mg  in 1 mL
Other Ingredients
Ingredient Kind Ingredient Name Quantity
May contain HYDROCHLORIC ACID (UNII: QTT17582CB)  
May contain SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52533-001-16 2 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 12/05/2011
Labeler - Cantrell Drug Company (035545763)

Revised: 5/2014
Document Id: 2a80c18a-119b-4df9-a9d2-b9bf8038d900
Set id: d9cd30df-4888-4041-8416-b59ecd89a063
Version: 7
Effective Time: 20140502
 
Cantrell Drug Company