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Effervescent Potassium Chloride
Effervescent Potassium Chloride - 0603-3508-16 - (Potassium Bicarbonate and Potassium Chloride Effervescent Tablets for Oral Solution)
Drug Information of Effervescent Potassium Chloride
| Product NDC: | 0603-3508 |
| Proprietary Name: | Effervescent Potassium Chloride |
| Non Proprietary Name: | Potassium Bicarbonate and Potassium Chloride Effervescent Tablets for Oral Solution |
| Active Ingredient(s): | 1.5; .7; 1.25 g/1; g/1; g/1 & nbsp; Potassium Bicarbonate and Potassium Chloride Effervescent Tablets for Oral Solution |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Effervescent Potassium Chloride
| Product NDC: | 0603-3508 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060106 |
Package Information of Effervescent Potassium Chloride
| Package NDC: | 0603-3508-16 |
| Package Description: | 30 TABLET, EFFERVESCENT in 1 BOX (0603-3508-16) |
NDC Information of Effervescent Potassium Chloride
| NDC Code | 0603-3508-16 |
| Proprietary Name | Effervescent Potassium Chloride |
| Package Description | 30 TABLET, EFFERVESCENT in 1 BOX (0603-3508-16) |
| Product NDC | 0603-3508 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Potassium Bicarbonate and Potassium Chloride Effervescent Tablets for Oral Solution |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20060106 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | LYSINE HYDROCHLORIDE; POTASSIUM BICARBONATE; POTASSIUM CHLORIDE |
| Strength Number | 1.5; .7; 1.25 |
| Strength Unit | g/1; g/1; g/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |
