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Potassium Bicarbonate
Potassium Bicarbonate - 0245-0039-30 - (Potassium Bicarbonate)
Drug Information of Potassium Bicarbonate
| 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) |
Labeler Information of Potassium Bicarbonate
| 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 Information of Potassium Bicarbonate
| Package NDC: | 0245-0039-30 |
| Package Description: | 30 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-30) |
NDC Information of Potassium Bicarbonate
| NDC Code | 0245-0039-30 |
| Proprietary Name | Potassium Bicarbonate |
| Package Description | 30 TABLET, EFFERVESCENT in 1 CARTON (0245-0039-30) |
| 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 |
