Label: DEXTROSE injection, solution
- NDC Code(s): 30798-127-17
- Packager: Durvet
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated November 7, 2019
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- DOSAGE & ADMINISTRATION
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CAUTIONS
Intravenous administration must be done slowly and made under stric asepsis. Solution should be warmed to body temperature prior to administration.
This is a single dose container. This product contains no preservative. After a quantity has been withdrawn for injection, the remainder should be discarded. Do not administer intraperitoneally
- ACTIVE INGREDIENTS:
- STORAGE AND HANDLING
- INDICATIONS:
- KEEP OUT OF REACH OF CHILDREN
- VETERINARY INDICATIONS
- SAFE HANDLING WARNING
- INFORMATION FOR OWNERS/CAREGIVERS
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
DEXTROSE
dextrose injection, solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:30798-127 Route of Administration INTRAVENOUS, INTRAMUSCULAR, INTRAPERITONEAL, SUBCUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30798-127-17 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/07/2019 Labeler - Durvet (056387798) Registrant - Durvet (056387798)