| NDC Code | 51662-1209-3 |
|---|
| Package Description | 10 POUCH in 1 CASE (51662-1209-3) / 1 CARTON in 1 POUCH (51662-1209-2) / 1 SYRINGE, GLASS in 1 CARTON / 10 mL in 1 SYRINGE, GLASS |
|---|
| Product NDC | 51662-1209 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Calcium Chloride |
|---|
| Non-Proprietary Name | Calcium Chloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAVENOUS; INTRAVENTRICULAR |
|---|
| Start Marketing Date | 20180913 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
|---|
| Substance Name | CALCIUM CHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
|---|