| Product NDC: | 0264-1940 |
| Proprietary Name: | POTASSIUM CHLORIDE |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 14.9 g/100mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | PARENTERAL |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0264-1940 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085870 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19780321 |
| Package NDC: | 0264-1940-10 |
| Package Description: | 12 CONTAINER in 1 CASE (0264-1940-10) > 500 mL in 1 CONTAINER |
| NDC Code | 0264-1940-10 |
| Proprietary Name | POTASSIUM CHLORIDE |
| Package Description | 12 CONTAINER in 1 CASE (0264-1940-10) > 500 mL in 1 CONTAINER |
| Product NDC | 0264-1940 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | PARENTERAL |
| Start Marketing Date | 19780321 |
| Marketing Category Name | ANDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 14.9 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |