| NDC Code | 31722-394-34 |
|---|
| Package Description | 25 VIAL, SINGLE-DOSE in 1 CARTON (31722-394-34) / 20 mL in 1 VIAL, SINGLE-DOSE (31722-394-20) |
|---|
| Product NDC | 31722-394 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Magnesium Sulfate |
|---|
| Non-Proprietary Name | Magnesium Sulfate Heptahydrate |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 20250528 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA219777 |
|---|
| Manufacturer | Camber Pharmaceuticals, Inc. |
|---|
| Substance Name | MAGNESIUM SULFATE HEPTAHYDRATE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
|---|