Home
>
National Drug Code (NDC)
>
Calcium Chloride
Calcium Chloride - 0409-1631-10 - (CALCIUM CHLORIDE)
Drug Information of Calcium Chloride
| Product NDC: | 0409-1631 |
| 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) |
Labeler Information of Calcium Chloride
| Product NDC: | 0409-1631 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021117 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110309 |
Package Information of Calcium Chloride
| Package NDC: | 0409-1631-10 |
| Package Description: | 10 CARTON in 1 CONTAINER (0409-1631-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC |
NDC Information of Calcium Chloride
| NDC Code | 0409-1631-10 |
| Proprietary Name | Calcium Chloride |
| Package Description | 10 CARTON in 1 CONTAINER (0409-1631-10) > 1 SYRINGE, PLASTIC in 1 CARTON > 10 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0409-1631 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CALCIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110309 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, 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] |
