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Potassium Chloride in Sodium Chloride
Potassium Chloride in Sodium Chloride - 0409-7116-09 - (SODIUM CHLORIDE and POTASSIUM CHLORIDE)
Drug Information of Potassium Chloride in Sodium Chloride
| Product NDC: | 0409-7116 |
| Proprietary Name: | Potassium Chloride in Sodium Chloride |
| Non Proprietary Name: | SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Active Ingredient(s): | 2.98; 9 g/1000mL; g/1000mL & nbsp; SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride in Sodium Chloride
| Product NDC: | 0409-7116 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019686 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19881017 |
Package Information of Potassium Chloride in Sodium Chloride
| Package NDC: | 0409-7116-09 |
| Package Description: | 12 POUCH in 1 CASE (0409-7116-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG |
NDC Information of Potassium Chloride in Sodium Chloride
| NDC Code | 0409-7116-09 |
| Proprietary Name | Potassium Chloride in Sodium Chloride |
| Package Description | 12 POUCH in 1 CASE (0409-7116-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG |
| Product NDC | 0409-7116 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM CHLORIDE and POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19881017 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | POTASSIUM CHLORIDE; SODIUM CHLORIDE |
| Strength Number | 2.98; 9 |
| Strength Unit | g/1000mL; g/1000mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
