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: | 0264-1940-20 |
Package Description: | 12 CONTAINER in 1 CASE (0264-1940-20) > 250 mL in 1 CONTAINER |
NDC Code | 0264-1940-20 |
Proprietary Name | POTASSIUM CHLORIDE |
Package Description | 12 CONTAINER in 1 CASE (0264-1940-20) > 250 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] |