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potassium phosphates
potassium phosphates - 0517-2350-25 - (Potassium Phosphate, Monobasic and Potassium Phosphate, Dibasic)
Drug Information of potassium phosphates
| Product NDC: | 0517-2350 |
| Proprietary Name: | potassium phosphates |
| Non Proprietary Name: | Potassium Phosphate, Monobasic and Potassium Phosphate, Dibasic |
| Active Ingredient(s): | 236; 224 mg/mL; mg/mL & nbsp; Potassium Phosphate, Monobasic and Potassium Phosphate, Dibasic |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of potassium phosphates
| Product NDC: | 0517-2350 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19891119 |
Package Information of potassium phosphates
| Package NDC: | 0517-2350-25 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2350-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of potassium phosphates
| NDC Code | 0517-2350-25 |
| Proprietary Name | potassium phosphates |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2350-25) > 50 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-2350 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Phosphate, Monobasic and Potassium Phosphate, Dibasic |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19891119 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | American Regent, Inc. |
| Substance Name | POTASSIUM PHOSPHATE, DIBASIC; POTASSIUM PHOSPHATE, MONOBASIC |
| Strength Number | 236; 224 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |
