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] |