Label: CALCIUM GLUCONATE injection, solution
- NDC Code(s): 65207-802-50
- Packager: Nova-Tech, 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.
Updated March 19, 2020
If you are a consumer or patient please visit this version.
- DOSAGE & ADMINISTRATION
- INFORMATION FOR OWNERS/CAREGIVERS
- Each 500 mL Contains
- STORAGE AND HANDLING
- GENERAL PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
calcium gluconate injection, solution
Product Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:65207-802 Route of Administration INTRAVENOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM GLUCONATE (UNII: SQE6VB453K) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM GLUCONATE 23 g in 100 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65207-802-50 500 mL in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/19/2020 Labeler - Nova-Tech, Inc. (196078976) Registrant - Nova-Tech, Inc. (196078976) Establishment Name Address ID/FEI Business Operations Nova-Tech, Inc. 196078976 manufacture