Home
>
National Drug Code (NDC)
>
Potassium Chloride
Potassium Chloride - 0904-1007-16 - (Potassium Chloride)
Drug Information of Potassium Chloride
| Product NDC: | 0904-1007 |
| Proprietary Name: | Potassium Chloride |
| Non Proprietary Name: | Potassium Chloride |
| Active Ingredient(s): | 40 meq/30mL & nbsp; Potassium Chloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride
| Product NDC: | 0904-1007 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081230 |
Package Information of Potassium Chloride
| Package NDC: | 0904-1007-16 |
| Package Description: | 473 mL in 1 BOTTLE (0904-1007-16) |
NDC Information of Potassium Chloride
| NDC Code | 0904-1007-16 |
| Proprietary Name | Potassium Chloride |
| Package Description | 473 mL in 1 BOTTLE (0904-1007-16) |
| Product NDC | 0904-1007 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Chloride |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20081230 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 40 |
| Strength Unit | meq/30mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
