MEPERIDINE HCL - meperidine 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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Meperidine HCl 10 mg/mL in 0.9% Sodium Chloride 50 mL Syringe

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MEPERIDINE HCL 
meperidine hcl injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-042
Route of Administration INTRAVENOUS DEA Schedule CII    
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEPERIDINE HYDROCHLORIDE (UNII: N8E7F7Q170) (MEPERIDINE - UNII:9E338QE28F) MEPERIDINE HYDROCHLORIDE 10 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Chloride (UNII: 451W47IQ8X) 9 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
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:52533-042-04 50 mL in 1 SYRINGE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 01/23/2012
Labeler - Cantrell Drug Company (035545763)
Establishment
Name Address ID/FEI Business Operations
Cantrell Drug Company 035545763 manufacture(52533-042) , human drug compounding outsourcing facility(52533-042) (No intent to compound 506E (drug shortage) drugs), (Not compounding from bulk ingredient)

Revised: 4/2014
Document Id: 5803ba3e-9045-438b-a68b-5ff868855e45
Set id: 8c11ffb8-6ff6-473c-b613-e8936e161a00
Version: 5
Effective Time: 20140430
 
Cantrell Drug Company