| NDC Code | 39822-0190-1 |
|---|
| Package Description | 1 VIAL, GLASS in 1 CARTON (39822-0190-1) / 5 mL in 1 VIAL, GLASS |
|---|
| Product NDC | 39822-0190 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Acetazolamide |
|---|
| Non-Proprietary Name | Acetazolamide |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20081210 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040784 |
|---|
| Manufacturer | XGen Pharmaceuticals DJB, Inc. |
|---|
| Substance Name | ACETAZOLAMIDE SODIUM |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS] |
|---|