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Potassium Chloride
Potassium Chloride - 63323-965-10 - (POTASSIUM CHLORIDE)
Drug Information of Potassium Chloride
| Product NDC: | 63323-965 |
| Proprietary Name: | Potassium Chloride |
| Non Proprietary Name: | POTASSIUM CHLORIDE |
| Active Ingredient(s): | 2 meq/mL & nbsp; POTASSIUM CHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Potassium Chloride
| Product NDC: | 63323-965 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA088901 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990927 |
Package Information of Potassium Chloride
| Package NDC: | 63323-965-10 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-965-10) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Potassium Chloride
| NDC Code | 63323-965-10 |
| Proprietary Name | Potassium Chloride |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-965-10) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 63323-965 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM CHLORIDE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19990927 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | POTASSIUM CHLORIDE |
| Strength Number | 2 |
| Strength Unit | meq/mL |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
