Label: DEXTROSE injection, solution
- NDC Code(s): 11695-1597-3
- Packager: Covetrus
- 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 December 27, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Dosage And Administration:
- Caution:
- GENERAL PRECAUTIONS
- Active Ingredients:
- Inactive Ingredients:
- STORAGE AND HANDLING
- GENERAL PRECAUTIONS
-
INFORMATION FOR OWNERS/CAREGIVERS
NDC: 11695-1597-3
18-801
RMS 92-1024Volume: 16.907 (500 mL)
Questions? (855) 724-3461
Reorder #069168
Manufactured by:
Nova-Tech, Inc.
Grand Island, NE 68801Distributed by:
Covetrus North America400 Metro Place North
Dublin, OH 43017
covetrus.com
Made in the USA
AH-069168-L-02
Rev: 0523Lot No. Exp. Date
- Indications:
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DEXTROSE
dextrose injection, solutionProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:11695-1597 Route of Administration INTRAVENOUS 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:11695-1597-3 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 06/21/2017 Labeler - Covetrus (603750329) Registrant - Covetrus (603750329) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture, api manufacture