Product NDC: | 0548-3304 |
Proprietary Name: | Calcium Chloride |
Non Proprietary Name: | Calcium Chloride |
Active Ingredient(s): | 100 mg/mL & nbsp; Calcium Chloride |
Administration Route(s): | PARENTERAL |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0548-3304 |
Labeler Name: | Amphastar Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20000601 |
Package NDC: | 0548-3304-00 |
Package Description: | 10 SYRINGE in 1 CARTON (0548-3304-00) > 10 mL in 1 SYRINGE |
NDC Code | 0548-3304-00 |
Proprietary Name | Calcium Chloride |
Package Description | 10 SYRINGE in 1 CARTON (0548-3304-00) > 10 mL in 1 SYRINGE |
Product NDC | 0548-3304 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcium Chloride |
Dosage Form Name | INJECTION |
Route Name | PARENTERAL |
Start Marketing Date | 20000601 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Amphastar Pharmaceuticals, Inc. |
Substance Name | CALCIUM CHLORIDE |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient] |