Product NDC: | 0264-7636 |
Proprietary Name: | Potassium Chloride in Dextrose and Sodium Chloride |
Non Proprietary Name: | DEXTROSE, SODIUM CHLORIDE, and POTASSIUM CHLORIDE |
Active Ingredient(s): | 5; .22; .45 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: | 0264-7636 |
Labeler Name: | B. Braun Medical Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019630 |
Marketing Category: | NDA |
Start Marketing Date: | 19880217 |
Package NDC: | 0264-7636-00 |
Package Description: | 12 CONTAINER in 1 CASE (0264-7636-00) > 1000 mL in 1 CONTAINER |
NDC Code | 0264-7636-00 |
Proprietary Name | Potassium Chloride in Dextrose and Sodium Chloride |
Package Description | 12 CONTAINER in 1 CASE (0264-7636-00) > 1000 mL in 1 CONTAINER |
Product NDC | 0264-7636 |
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 | 5; .22; .45 |
Strength Unit | g/100mL; g/100mL; g/100mL |
Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |