lectrolyte #1
Travert 10% Electrolyte #2
Travert 10% Electrolyte #3
Only those solutions listed above should be used for the intravenous infusion of Oxacillin Sodium. The concentration of the antibiotic should fall within the range specified. The drug concentration and the rate and volume of the infusion should be adjusted so that the total dose of oxacillin is administered before the drug loses its stability in the solution in use.
If another agent is used in conjunction with oxacillin therapy, it should not be physically mixed with oxacillin but should be administered separately.
Pharmacy Bulk Package
This glass vial contains 10 grams Oxacillin Sodium and is designed for use in the pharmacy in preparing IV admixtures. Add 93 mL Sterile Water for Injection, USP or Sodium Chloride Injection, USP 0.9%. The resulting solution will contain 100 mg oxacillin per mL and will require further dilution.
CAUTION: NOT TO BE DISPENSED AS A UNIT.
Directions For Proper Use of Pharmacy Bulk Package
The container closure may be penetrated only one time after reconstitution, utilizing a suitable sterile dispensing set which allows measured distribution of the contents.
Use of this product is restricted to a suitable work area, such as a laminar flow hood.
Once this container closure has been punctured, withdrawal of the contents should be completed without delay. If prompt fluid transfer cannot be accomplished, discard the contents no later than 4 hours after initial closure puncture.
A plastic ball attached to the pharmacy bulk package provides a suitable hanging device while dispensing contents.
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
HOW SUPPLIED
Oxacillin for Injection, USP, is available in a pharmacy bulk package which contains oxacillin sodium monohydrate equivalent to 10 grams oxacillin.
NDC 0781-3103-95 10 grams Pharmacy Bulk Package, 100 mL, Packaged in 10s
Storage
Store the dry powder at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature].
08-2009
46018657
Manufactured in Austria by Sandoz GmbH
for Sandoz Inc., Princeton, NJ 08540
PRINCIPAL DISPLAY PANEL
10 gram Vial
NDC 0781-3103-46
Oxacillin
for Injection, USP
Buffered - For IM or IV use*
10 grams Rx only
SANDOZ
OXACILLIN
oxacillin injection, powder, for solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0781-3103
Route of Administration INTRAMUSCULAR, INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXACILLIN SODIUM (OXACILLIN) OXACILLIN SODIUM 10 g
Inactive Ingredients
Ingredient Name Strength
SODIUM PHOSPHATE, DIBASIC
Product Characteristics
Color Score
Shape Size
Flavor Imprint Code
Contains
Packaging
NDC Package Description Multilevel Packaging
1 0781-3103-95 10 VIAL In 1 PACKAGE contains a VIAL, PHARMACY BULK PACKAGE (0781-3103-46)
1 0781-3103-46 1 VIAL In 1 VIAL, PHARMACY BULK PACKAGE This package is contained within the PACKAGE (0781-3103-95)
Marketing Information
Marketing Category Application Number or Mon |
