| Product NDC: | 0603-4170 |
| Proprietary Name: | K-EFFERVESCENT |
| Non Proprietary Name: | POTASSIUM BICARBONATE |
| Active Ingredient(s): | 25 meq/1 & nbsp; POTASSIUM BICARBONATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EFFERVESCENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0603-4170 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20060106 |
| Package NDC: | 0603-4170-16 |
| Package Description: | 30 TABLET, EFFERVESCENT in 1 BOX (0603-4170-16) |
| NDC Code | 0603-4170-16 |
| Proprietary Name | K-EFFERVESCENT |
| Package Description | 30 TABLET, EFFERVESCENT in 1 BOX (0603-4170-16) |
| Product NDC | 0603-4170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | POTASSIUM BICARBONATE |
| Dosage Form Name | TABLET, EFFERVESCENT |
| Route Name | ORAL |
| Start Marketing Date | 20060106 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | POTASSIUM BICARBONATE |
| Strength Number | 25 |
| Strength Unit | meq/1 |
| Pharmaceutical Classes | Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |