Product NDC: | 0517-2710 |
Proprietary Name: | Calcium Chloride |
Non Proprietary Name: | Calcium Chloride |
Active Ingredient(s): | 100 mg/mL & nbsp; Calcium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-2710 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19900930 |
Package NDC: | 0517-2710-25 |
Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2710-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0517-2710-25 |
Proprietary Name | Calcium Chloride |
Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2710-25) > 10 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0517-2710 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19900930 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | American Regent, Inc. |
Substance Name | CALCIUM CHLORIDE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Calcium [Chemical/Ingredient],Calcium [EPC],Phosphate Binder [EPC],Phosphate Chelating Activity [MoA] |