| NDC Code | 23155-831-31 | 
|---|
			| Package Description | 1 VIAL, GLASS in 1 CARTON (23155-831-31)  / 5 mL in 1 VIAL, GLASS | 
|---|
			| Product NDC | 23155-831 | 
|---|
			| 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 | 20221115 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA202693 | 
|---|
			| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | 
|---|
			| Substance Name | ACETAZOLAMIDE SODIUM | 
|---|
			| Strength | 500 | 
|---|
			| Strength Unit | mg/5mL | 
|---|
			| Pharmacy Classes | Carbonic Anhydrase Inhibitor [EPC], Carbonic Anhydrase Inhibitors [MoA], Sulfonamides [CS] | 
|---|