| NDC Code | 63323-099-63 |
|---|
| Package Description | 10 VIAL, PLASTIC in 1 TRAY (63323-099-63) / 200 mL in 1 VIAL, PLASTIC (63323-099-03) |
|---|
| Product NDC | 63323-099 |
|---|
| 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 | 20230711 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA217796 |
|---|
| Manufacturer | Fresenius Kabi USA, LLC |
|---|
| Substance Name | SODIUM CHLORIDE |
|---|
| Strength | 4 |
|---|
| Strength Unit | meq/mL |
|---|
| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
|---|