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Potassium Acetate
Potassium Acetate - 0517-5024-25 - (Potassium Acetate)
Drug Information of Potassium Acetate
| Product NDC: | 0517-5024 |
| Proprietary Name: | Potassium Acetate |
| Non Proprietary Name: | Potassium Acetate |
| Active Ingredient(s): | 392 mg/mL & nbsp; Potassium Acetate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Acetate
| Product NDC: | 0517-5024 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19900930 |
Package Information of Potassium Acetate
| Package NDC: | 0517-5024-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5024-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Potassium Acetate
| NDC Code | 0517-5024-25 |
| Proprietary Name | Potassium Acetate |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5024-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-5024 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Acetate |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900930 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | POTASSIUM ACETATE |
| Strength Number | 392 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
