- PRECAUTIONS
- INDICATIONS:
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DOSAGE AND ADMINISTRATION:
May be injected intravenously, subcutaneously or intraperitoneally (except in horses) using strict aseptic technique.
Cattle and Horses: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
Swine and Sheep: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.
If administered subcutaneously divide the dosage into several sites of injection and massage points of injection to aid in absorption and help prevent inflammation and/or sloughing.
- STORAGE AND HANDLING
- INFORMATION FOR OWNERS/CAREGIVERS
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DOSAGE FORMS & STRENGTHS
Each 100 mL contains:
Sodium Chloride..................600 mg
Sodium Lactate...................310 mg
Potassium Chloride...............30 mg
Calcium Chloride Dihydrate....20 mg
Water for Injection...................q.s.
The Calcium, Potassium and Sodium contents are approximately 2.7, 4.0, and 130 mEq/liter, respectively.
Total Osmolar Concentration: 269 mOsm per liter (calculated). - CAUTION:
- WARNING:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LACTATED RINGERS
lactated ringers injection, solutionProduct Information Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:60270-858 Route of Administration INTRAVENOUS, SUBCUTANEOUS, INTRAPERITONEAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 600 mg in 100 mL SODIUM LACTATE (UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) SODIUM LACTATE 310 mg in 100 mL POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 30 mg in 100 mL CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CHLORIDE 20 mg in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60270-858-20 1000 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/31/2012 Labeler - VetTek (056387798) Registrant - VetTek (056387798) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture