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AcetaZOLAMIDE
AcetaZOLAMIDE - 55390-460-01 - (Acetazolamide)
Drug Information of AcetaZOLAMIDE
| Product NDC: | 55390-460 |
| Proprietary Name: | AcetaZOLAMIDE |
| Non Proprietary Name: | Acetazolamide |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetazolamide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AcetaZOLAMIDE
| Product NDC: | 55390-460 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040089 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960501 |
Package Information of AcetaZOLAMIDE
| Package NDC: | 55390-460-01 |
| Package Description: | 1 VIAL in 1 BOX, UNIT-DOSE (55390-460-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
NDC Information of AcetaZOLAMIDE
| NDC Code | 55390-460-01 |
| Proprietary Name | AcetaZOLAMIDE |
| Package Description | 1 VIAL in 1 BOX, UNIT-DOSE (55390-460-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
| Product NDC | 55390-460 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Acetazolamide |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19960501 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | ACETAZOLAMIDE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA],Sulfonamides [Chemical/Ingredient] |
