| Product NDC: | 0264-7865 |
| Proprietary Name: | POTASSIUM CHLORIDE IN SODIUM CHLORIDE |
| Non Proprietary Name: | SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Active Ingredient(s): | .15; .9 g/100mL; g/100mL & nbsp; SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0264-7865 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019708 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890929 |
| Package NDC: | 0264-7865-00 |
| Package Description: | 12 CONTAINER in 1 CASE (0264-7865-00) > 1000 mL in 1 CONTAINER |
| NDC Code | 0264-7865-00 |
| Proprietary Name | POTASSIUM CHLORIDE IN SODIUM CHLORIDE |
| Package Description | 12 CONTAINER in 1 CASE (0264-7865-00) > 1000 mL in 1 CONTAINER |
| Product NDC | 0264-7865 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19890929 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | POTASSIUM CHLORIDE; SODIUM CHLORIDE |
| Strength Number | .15; .9 |
| Strength Unit | g/100mL; g/100mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |