LIDOCAINE: Product Information

LIDOCAINE- lidocaine hydrochloride injection
Vedco, Inc.

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.

CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

Lidocaine is a potent local anesthetic for producing epidural, nerve conduction and infiltration anesthesia.

CONTRAINDICATIONS

Lidocaine is contraindicated in animals with a known hypersensitivity to the drug.

PRECAUTIONS

Lidocaine is usually well tolerated. Nevertheless, as with all local anesthetics, untoward effects may occur due to hypersensitivity, faulty technique, overdosage and inadvertent intravascular or subarachnoid injection. In case of respiratory arrest, immediate resuscitation with oxygen is indicated.

DOSAGE AND ADMINISTRATION

Epidural
Cattle and Horses — 5 to 15 mL
Dogs and Cats — 1 mL per 10 pounds of body weight.
Nerve Block
Cattle and Horses — 5 to 20 mL
Infiltration
Dilute to 0.5% concentration (1 mL of 2% solution diluted with 3 mL of sterile water = 4 mL of a 0.5% solution)

COMPOSITION

Each mL of sterile aqueous solution contains:
Lidocaine Hydrochloride……………………2.0%
Propylene Glycol…………………………….5.2%
Sodium Chloride……………………………..0.5%
Sodium Lactate………………………………0.5%
with Methylparaben 0.15%, Sodium Metabisulfite 0.10%,
Propylparaben 0.03%, and Disodium Edetate 0.001% as preservatives.

Store at controlled room temperature between 15^o and 30^o C (59^o -86^o F)

TAKE TIME OBSERVE LABEL DIRECTIONS

LIDOCAINE lidocaine injection

Product Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:50989-417 Route of Administration EPIDURAL, INFILTRATION DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LIDOCAINE HYDROCHLORIDE (Lidocaine) LIDOCAINE HYDROCHLORIDE ANHYDROUS 0.02 g in 1 mL

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:50989-417-12 100 mL in 1 BOTTLE None 2 NDC:50989-417-15 250 mL in 1 BOTTLE None

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/1995

Labeler — Vedco, Inc. (021634266)

Revised: 04/2018 Vedco, Inc.