MANNITOL 20%- mannitol injection
Clipper
Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
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Mannitol Injection 20% is indicated for use as an osmotic diuretic in canine species. Mannitol is essentially inert metabolically. When given parenterally, it is freely filtered at the glomerulus which produces osmotic diuresis as more than 90% of the mannitol injected escapes reabsorption.
Mannitol USP...................................20 g
Water for Injection...........................q.s.
This solution contains 1098 mOsmols/Liter
The usual canine dosage administered intravenously is 1.5 - 2.0 g per Kg body weight given over a 30 minute period. This is approximately 3.4-4.5 mL/lb of body weight.
Crystals of mannitol may form in a 20% saturated solution of mannitol. Dissolve the crystals by warming in hot water or autoclaving for 15 minutes. Cool to body temperature before administering. This is a single dose vial that contains no preservatives. Use entire contents when first opened or resterilize by autoclaving.
Manufactured by: Nova-Tech, Inc. Grand Island, NE 68801 for Neogen Corporation
Item No. 09061
1072-022114
Lot No.:
Exp. Date
NDC: 57319-521-05
Mannitol Injection 20%
Sterile Solution
Net Contentes: 100 mL
PhoenixTM
Manufactured for:
Clipper Distributing Company, LLC.
St. Joseph, MO 64507
Trademares are property of Clipper Distributing Company, LLC
MANNITOL 20%
mannitol injection |
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Labeler - Clipper (150711039) |
Registrant - Nova-Tech, Inc (196078976) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Nova-Tech, Inc | 196078976 | manufacture |