| NDC Code | 0409-1141-25 |
|---|
| Package Description | 25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-25) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
|---|
| Product NDC | 0409-1141 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Sodium Chloride |
|---|
| Non-Proprietary Name | Sodium Chloride |
|---|
| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20170619 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | Hospira, Inc. |
|---|
| Substance Name | SODIUM CHLORIDE |
|---|
| Strength | 234 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
|---|