LIDOCAINE HCL- lidocaine hcl 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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Lidocaine HCl 2% Injection Solution 5 mL Syringe

• WARNINGS AND PRECAUTIONS

Outsourced Compounded Drug. Not for Resale. Hospital/Office Use Only.

• ADVERSE EVENTS

To facilitate Adverse Event Reporting: www.fda.gov/medwatch or 1-800-FDA-1088.

• HOW SUPPLIED

Lidocaine Hydrochloride is supplied as a sterile, nonpyrogenic solution that is clear, colorless in a 5 mL Single-Dose Syringe.

This product is Preservative-Free and Latex-Free.

• INGREDIENTS

Each 1 mL contains 20 mg Lidocaine Hydrochloride and 6 mg Sodium Chloride in Sterile Water for Injection q.s. The aqueous solution is adjusted to a pH of 6.5 (5.0- 7.0) with hydrochloric acid and/or sodium hydroxide, if necessary.

• STORAGE AND HANDLING

Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]. 

• DOSAGE AND ADMINISTRATION.

FOR LOCAL ANESTHETIC USE. PRESERVATIVE-FREE INJECTION SOLUTION.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.  Solutions that are discolored and/or contain particulate matter should not be used.

Rx Only


Rev. 02/15


CANTRELL DRUG COMPANY

LITTLE ROCK, AR 72207

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LIDOCAINE HCL 
lidocaine hcl injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:52533-153
Route of AdministrationINFILTRATION
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 6 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52533-153-155 mL in 1 SYRINGE, PLASTIC; Type 0: Not a Combination Product02/25/201512/06/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/25/201512/06/2017
Labeler - Cantrell Drug Company (035545763)

Revised: 12/2017
 
Cantrell Drug Company