Ceftiofur sodium
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Ceftiofur sodium
FULL PRESCRIBING INFORMATION
Ceftiofur sodium
Ceftiofur sodium POWDER
Product Information
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Product Type
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Bulk ingredient |
Item Code (Source)
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NDC:58597-8170 |
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Route of Administration
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NOT APPLICABLE |
DEA Schedule
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Active Ingredient/Active Moiety
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Ingredient Name
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Basis of Strength
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Strength
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Ceftiofur sodium ceftiofur |
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1 g
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Packaging
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#
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Item Code
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Package Description
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Marketing Start Date
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Marketing End Date
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1 |
NDC:58597-8170-9 |
5000 in 1 BOTTLE |
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Marketing Information
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Marketing Category
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Application Number or Monograph Citation
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Marketing Start Date
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Marketing End Date
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2014-04-25 |
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PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
