Product NDC: | 0245-0039 |
Proprietary Name: | Potassium Bicarbonate |
Non Proprietary Name: | Potassium Bicarbonate |
Active Ingredient(s): | 2.5 g/1 & nbsp; Potassium Bicarbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, EFFERVESCENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0245-0039 |
Labeler Name: | Upsher-Smith Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20021201 |
Package NDC: | 0245-0039-01 |
Package Description: | 100 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-01) |
NDC Code | 0245-0039-01 |
Proprietary Name | Potassium Bicarbonate |
Package Description | 100 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-01) |
Product NDC | 0245-0039 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Potassium Bicarbonate |
Dosage Form Name | TABLET, EFFERVESCENT |
Route Name | ORAL |
Start Marketing Date | 20021201 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Upsher-Smith Laboratories, Inc. |
Substance Name | POTASSIUM BICARBONATE |
Strength Number | 2.5 |
Strength Unit | g/1 |
Pharmaceutical Classes |