Oxacillin Injection, Powder, For Solution
Product Images NDC 64679-698

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Oxacillin (NDC 64679-698). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wockhardt Usa Llc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

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FDA Label Image

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This is a description of a vial containing Oxacillin Sodium, a medication used for intravenous or intramuscular injection. The vial is buffered and contains 1 gram of Oxacillin and 21 mg of basic sodium phosphate. The recommended dosage for adults is 250 mg to 500 mg intramuscularly every 4 to 6 hours, and there are instructions for intravenous use in the insert. The vial should be discarded after 3 days at room temperature or 7 days under refrigeration. The medication is manufactured by Wockhardt USA LLC and the address of the manufacturer is provided.*

FDA Label Image

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This is a medication labeled as an equivalent of Oxacillin for Injection, USP. It contains 2 grams of Oxacillin and 42 mg of dibasic sodum phosphate in a buffered solution. The recommended dosage for adults is 250 mg to 500 mg administered every 4 to 6 hours through an injection, based on the accompanying insert. The medication is for IM or IV use only and should be discarded if not used within 3 days at room temperature or 7 days under refrigeration. It is manufactured by Mim S. Vioekra USA, LLC and distributed by Watoow B, Parsgpany, NI.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.