NDC Code | 39822-0190-7 |
Package Description | 1 VIAL, GLASS in 1 CARTON (39822-0190-7) > 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 | 20131210 |
Marketing Category Name | ANDA |
Application Number | ANDA040784 |
Manufacturer | X-GEN Pharmaceuticals, Inc. |
Substance Name | ACETAZOLAMIDE SODIUM |
Strength | 500 |
Strength Unit | mg/5mL |
Pharmacy Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [CS] |