Product NDC: | 52533-102 |
Proprietary Name: | Calcium Chloride |
Non Proprietary Name: | Calcium Chloride |
Active Ingredient(s): | 20 mg/mL & nbsp; Calcium Chloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-102 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110308 |
Package NDC: | 52533-102-43 |
Package Description: | 50 mL in 1 BAG (52533-102-43) |
NDC Code | 52533-102-43 |
Proprietary Name | Calcium Chloride |
Package Description | 50 mL in 1 BAG (52533-102-43) |
Product NDC | 52533-102 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcium Chloride |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20110308 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Cantrell Drug Company |
Substance Name | CALCIUM CHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient] |