| Product NDC: | 0264-7663 |
| Proprietary Name: | Potassium Chloride in Dextrose and Sodium Chloride |
| Non Proprietary Name: | DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
| Active Ingredient(s): | 10; .15; .2 g/100mL; g/100mL; g/100mL & nbsp; DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0264-7663 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019630 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880217 |
| Package NDC: | 0264-7663-20 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-7663-20) > 250 mL in 1 CONTAINER |
| NDC Code | 0264-7663-20 |
| Proprietary Name | Potassium Chloride in Dextrose and Sodium Chloride |
| Package Description | 24 CONTAINER in 1 CASE (0264-7663-20) > 250 mL in 1 CONTAINER |
| Product NDC | 0264-7663 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19880217 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
| Strength Number | 10; .15; .2 |
| Strength Unit | g/100mL; g/100mL; g/100mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |