Home
>
National Drug Code (NDC)
>
Acetazolamide
Acetazolamide - 25021-817-10 - (acetazolamide sodium)
Drug Information of Acetazolamide
| Product NDC: | 25021-817 |
| Proprietary Name: | Acetazolamide |
| Non Proprietary Name: | acetazolamide sodium |
| Active Ingredient(s): | 500 mg/5mL & nbsp; acetazolamide sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acetazolamide
| Product NDC: | 25021-817 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200880 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120615 |
Package Information of Acetazolamide
| Package NDC: | 25021-817-10 |
| Package Description: | 1 VIAL in 1 CARTON (25021-817-10) > 5 mL in 1 VIAL |
NDC Information of Acetazolamide
| NDC Code | 25021-817-10 |
| Proprietary Name | Acetazolamide |
| Package Description | 1 VIAL in 1 CARTON (25021-817-10) > 5 mL in 1 VIAL |
| Product NDC | 25021-817 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | acetazolamide sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120615 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | ACETAZOLAMIDE SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [Chemical/Ingredient] |
