Label: DEXTROSE injection, solution
- NDC Code(s): 29983-2403-1
- Packager: IBA Inc.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated January 16, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- INDICATIONS:
- DOSAGE and ADMINISTRATION:
- VETERINARY INDICATIONS
- STORAGE AND HANDLING
- WARNINGS AND PRECAUTIONS
- CONTAINS:
- WARNINGS
- NOTE:
- CAUTION:
- INFORMATION FOR OWNERS/CAREGIVERS
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DEXTROSE
dextrose injection, solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:29983-2403 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 250 g in 500 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:29983-2403-1 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/16/2018 Labeler - IBA Inc. (019494160) Registrant - IBA Inc. (019494160) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture, api manufacture