Veterinary PLASMA-LYTE A: Product Information (Page 2 of 2)

Preparation for Administration

  1. Suspend container from eyelet support.
  2. Remove plastic protector from outlet port at bottom of container.
  3. Attach administration set. Refer to complete directions accompanying

image description
(click image for full-size original)

Container Label

Veterinary PLASMA-LYTE A

Injection pH 7.4

(Multiple Electrolytes Injection Type 1 USP)

5000 mL

Each 100 mL Contains 526 mg Sodium Chloride

USP 502 mg Sodium Gluconate USP 368 mg Sodium

Acetate Trihydrate USP 37 mg Potassium Chloride

USP 30 mg Magnesium chloride usp pH adjusted

with Sodium Hydroxide pH 7.4 (6.5 to 8.0) mEq/L

Sodium 140 Potassium 5 Magnesium 3 Chloride 98

Acetate 27 Gluconate 23 Osmolarity 294 mOsmol/L

(calc) Sterile Nonpyrogenic SinglGLe dose container

Contains no antimicrobial agents Use solution promptly

Following initial entry Additives may be incompatible

Consult with pharmacist if available When introducing

additives use aseptic technique Mix thoroughly Discard

unused portion Dosage Intravenously as directed by

a veterinarian See package insert Cautions Squeeze

and inspect inner bag which maintains product sterility

Discard if leaks are found Do not use unless solution

is clear and seal is intact Store unit in moisture

barrier overwrap at room temperature (25°C/77°F)

until ready to use Avoid excessive heat

For animal use only

Caution Federal (usa) law restricts this drug to use by

or on the order of a licensed veterinarian

Baxter and Plasma-lyte are trademarks

of Baxter International, Inc.

For customer service call

NDC 0338-0090-02

800 933 0303

2B8229

Baxter Healthcare Corporation

Made in USA

Baxter Logo

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VETERINARY PLASMA-LYTE A sodium chloride, sodium gluconate, sodium acetate, potassium chloride, magnesium chloride injection, solution
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:0338-0090
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SODIUM CHLORIDE (CHLORIDE ION and SODIUM CATION) SODIUM CHLORIDE 526 mg in 100 mL
SODIUM GLUCONATE (GLUCONIC ACID and SODIUM CATION) SODIUM GLUCONATE 502 mg in 100 mL
SODIUM ACETATE (ACETATE ION and SODIUM CATION) SODIUM ACETATE 368 mg in 100 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 37 mg in 100 mL
MAGNESIUM CHLORIDE (MAGNESIUM CATION and CHLORIDE ION) MAGNESIUM CHLORIDE 30 mg in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0338-0090-02 2 BAG in 1 CARTON contains a BAG
1 5000 mL in 1 BAG This package is contained within the CARTON (0338-0090-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 05/21/2019
Labeler — Baxter Healthcare Corporation (005083209)
Establishment
Name Address ID/FEI Operations
Baxter Healthcare Corporation 059140764 analysis, label, manufacture, pack, sterilize, api manufacture
Establishment
Name Address ID/FEI Operations
Baxter Healthcare Corporation 194684502 analysis
Establishment
Name Address ID/FEI Operations
Baxter, S.A. de C.V. 810432484 analysis, label, manufacture, pack, sterilize

Revised: 07/2020 Baxter Healthcare Corporation

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