Hexasol Recall

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Questions & Answers

Side Effects & Adverse Reactions

There is currently no warning information available for this product. We apologize for any inconvenience.

Legal Issues

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FDA Safety Alerts

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Manufacturer Warnings

There is currently no manufacturer warning information available for this drug.

FDA Labeling Changes

There are currently no FDA labeling changes available for this drug.


For the treatment of bacterial pneumonia associated with Pasteurella spp. and for the control of associated pyrexia in beef and non-lactating dairy cattle.


There is currently no drug history available for this drug.

Other Information

Hexasol™ Injection is a sterile, pre-constituted solution of the broad-spectrum antibiotic oxytetracycline dihydrate and the non-steroidal anti-inflammatory drug (NSAID) flunixin meglumine. Each mL contains 300 mg of oxytetracycline base as amphoteric oxytetracycline; 20 mg of flunixin base as flunixin meglumine, 40% (v/v) glycerol formal, 10% (v/v) polyethylene glycol 200, 2.7% (w/v) magnesium oxide, 0.4% (w/v) sodium formaldehyde sulphoxylate (as a preservative) and monoethanolamine (as required to adjust pH).

Hexasol Manufacturers

  • Norbrook Laboratories Limited
    Hexasol (Oxytetracycline, Flunixin Meglumine) Injection, Solution [Norbrook Laboratories Limited]

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